Laboratory Services List | Medi Linx Laboratory Inc.

24 Hours Urine Total Protein

The 24 hours Urine Total protein urine test measures the amount of protein in a sample of urine collected over 24 hours. Proteins are substances that are essential for the body to function properly and is normally found in the blood. Increase amounts of protein in urine may indicate kidney disease.

Source: medlineplus.gov

TEST DETAILS
MLLI CODE	J24UPA

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Benzethonium Chloride
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
24 hour urine	10 mL	17	Storage: 2 to 8˚C Stability: 7 days Storage: 20 to 25˚C Stability: 24 hours Storage: -20˚C Stability: 1 month	Avoid collection of specimens within 24 hours of intense exercise since this can falsely elevate protein excretion. During the start of collection, empty the bladder and discard the first urine output. Collect all the succeeding urine voided in a 24-hour period. Keep the urine container either in a refrigerator or in an ice chest.
NOTE	•If aliquoted sample, please indicate total volume in mL and specific gravity, date and time of start and end of collection.

Conventional Reference Range	Conventional Unit
Less than 300.00	mgs/24 Hour
International Reference Range	International Unit
Not Applicable	Not Applicable

2 Hours Post - Prandial Blood Sugar

This test measures blood glucose exactly 2 hours after a meal. It is extensively used to establish the diagnosis of diabetes mellitus. It aids along with FBS to follow up patients with impaired glucose tolerance.

Source: Glucose assay package insert

TEST DETAILS
MLLI CODE	J2PPBS

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Hexokinase/Glucose-6-phosphate dehydrogenase (G-6-PDH)
Synonyms	Not Applicable
Acronyms	2HR-PPBS - Post Prandial Blood Sugar

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days Storage: 20 to 25˚C Stability: 2 days Storage: -20˚C Stability: 1 day	Patient will take 75-gram glucose load or complete meal (breakfast or lunch) two hours prior to drawing of blood.
NOTE	None

Conventional Reference Range	Conventional Unit
64.87 to 138.75	mg/dL
International Reference Range	International Unit
3.6 to 7.7	mmol/L

24 Hour Urine Amylase

The Amylase urine test measures the amount of amylase in a sample of urine collected over 24 hours (24-hour urine test test). Amylase is produced in the pancreas and parotid glands. Elevated result may aid in the diagnosis of pancreatitis and other pancreatic disorders.

Source: Amylase assay package insert

TEST DETAILS
MLLI CODE	JAMU24

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	2-chloro-4-nitrophenyl-α-D-maltotrioside (CNPG3 Substrate)
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
24 hour urine	10 mL	17	Storage: 2 to 8 ⁰C Stability: 3 days Storage: 20 to 25 ⁰C Stability: 24 hours	During the start of collection, empty the bladder and discard the first urine output. Collect all the succeeding urine voided in a 24-hour period. Keep the urine container either in a refrigerator or in an ice chest.
NOTE	•If aliquoted sample, please indicate total volume in mL and specific gravity, date and time of start and end of collection.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

24 Hour Urine Calcium

"This test measures urinary calcium which reflects dietary intake and rate of calcium absorption collected for 24 hours. It is used to evaluate endocrine function, calcium metabolism and excretion, and acid–base balance. To guide therapy in patients with renal failure, renal transplant, endocrine disorders, malignancies, cardiac disease, and skeletal disorders. And to monitor treatment in calcium deficiency."

Source: Brunner and Suddarth's Handbook of Laboratory and Diagnostic Tests

TEST DETAILS
MLLI CODE	J24UCA

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Arsenazo III complex
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
24 hour urine	10 mL	17	Storage: 2 to 8˚C Stability: 4 days Storage: 20 to 25˚C Stability: 2 days Storage: -20˚C Stability: 3 weeks	During the start of collection, empty the bladder and discard the first urine output. Collect all the succeeding urine voided in a 24-hour period. Keep the urine container either in a refrigerator or in an ice chest.
NOTE	•If aliquoted sample, please indicate total volume in mL and specific gravity, date and time of start and end of collection. •Collect urine specimen with 10 mL distilled water and 10 mL hydrochloric acid as preservative (20 mL of 6 mol/L HCl)

Conventional Reference Range	Conventional Unit
2.50 to 7.50	mmol/24 Hour
International Reference Range	International Unit
Not Applicable	Not Applicable

24 Hour Urine Chloride

This test reevaluates renal conservation of electrolytes from a 24 hour urine collection. Its purpose is to help evaluate fluid and electrolyte imbalance, and renal and adrenal disorders.

Source: Brunner and Suddarth's Handbook of Laboratory and Diagnostic Tests

TEST DETAILS
MLLI CODE	J24UCL

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Ion-selective electrode diluted indirect
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
24 hour urine	10 mL	17	Storage: 2 to 8˚C Stability: 7 days Storage: 20 to 25˚C Stability: 7 days Storage: -20˚C Stability: 7 days	During the start of collection, empty the bladder and discard the first urine output. Collect all the succeeding urine voided in a 24-hour period. Keep the urine container either in a refrigerator or in an ice chest.
NOTE	•If aliquoted sample, please indicate total volume in mL and specific gravity, date and time of start and end of collection.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

24 Hour Urine Creatinine

This test is used to help assess the glomerular filtration function of the kidneys and to check the accuracy of 24-hour urine collection, based on the relatively constant levels of creatinine excretion.

Source: Brunner and Suddarth's Handbook of Laboratory and Diagnostic Tests

TEST DETAILS
MLLI CODE	J24UCR

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Enzymatic Quinoneimine
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
24 hour urine	10 mL	17	Storage: 2 to 8˚C Stability: 6 days Storage: 20 to 25˚C Stability: 2 days Storage: -20˚C Stability: 6 months	During the start of collection, empty the bladder and discard the first urine output. Collect all the succeeding urine voided in a 24-hour period. Keep the urine container either in a refrigerator or in an ice chest.
NOTE	•If aliquoted sample, please indicate total volume in mL and specific gravity, date and time of start and end of collection. •Collect urine specimen with 5 mL distilled water and 5 mL hydrochloric acid as preservative (6N of HCl).

Conventional Reference Range	Conventional Unit
Male: 871.02 to 2409.46 Female: 667.41 to 1594.99	mg/24 Hour
International Reference Range	International Unit
Male: 7.70 to 21.30 Female: 5.90 to 14.10	mmol/24 Hour

24 Hour Urine Magnesium

Renal urine magnesium testing is used in assessing the cause of abnormal serum magnesium concentration. It is also aids in determining whether nutritional magnesium. It may also help on assessing risk to kidney stones.

Source: mayocliniclabs.com

TEST DETAILS
MLLI CODE	J24MG

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Enzymatic
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
24 hour urine	10mL	17	Storage: 2 to 8˚C Stability: 3 days Storage: 20 to 25˚C Stability: 3 days Storage: -20˚C Stability: 1 year	During the start of collection, empty the bladder and discard the first urine output. Collect all the succeeding urine voided in a 24-hour period. Keep the urine container either in a refrigerator or in an ice chest.
NOTE	•If aliquoted sample, please indicate total volume in mL and specific gravity, date and time of start and end of collection. •Collect urine specimen with 10 mL distilled water and 10 mL hydrochloric acid as preservative (20 mL of 6 mol/L HCl)

Conventional Reference Range	Conventional Unit
72.9 to 121.5	mgs/24 Hour
International Reference Range	International Unit
Not Applicable	Not Applicable

24 Hour Urine Phosphorus

The phosphorous urine test is useful in evaluation increased and decreased levels of phosphatemic states. It also used in the monitroing of patient with nephrolithiasis.

Source: mayocliniclabs.com

TEST DETAILS
MLLI CODE	J24UPP

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Phosphomolybdate
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
24 hour urine	10 mL	17	Storage: 20 to 25˚C Stability: 2 days	During the start of collection, empty the bladder and discard the first urine output. Collect all the succeeding urine voided in a 24-hour period. Keep the urine container either in a refrigerator or in an ice chest.
NOTE	•If aliquoted sample, please indicate total volume in mL and specific gravity, date and time of start and end of collection. •Collect urine specimen with 10 mL distilled water and 10 mL hydrochloric acid as preservative (20 mL of 6 mol/L HCl)

Conventional Reference Range	Conventional Unit
0.40 to 1.30	g/24 Hour
International Reference Range	International Unit
12.90 to 42.00	mmol/24 Hour

24 Hour Urine Potassium

The kidneys provide the most important regulation of K+. Urine Potassium determination is useful in identification of cause for hyperkalemia or hypokalemia.

Source: mayocliniclabs.com

TEST DETAILS
MLLI CODE	J24UKU

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Ion-selective electrode diluted (Indirect)
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
24 hour urine	10 mL	17	Storage: 2 to 8˚C Stability: 2 months Storage: 20 to 25˚C Stability: 45 days Storage: -20˚C Stability: 1 year	During the start of collection, empty the bladder and discard the first urine output. Collect all the succeeding urine voided in a 24-hour period. Keep the urine container either in a refrigerator or in an ice chest.
NOTE	•If aliquoted sample, please indicate total volume in mL and specific gravity, date and time of start and end of collection.

Conventional Reference Range	Conventional Unit
25.00 – 125.00	mmol/24 Hour
International Reference Range	International Unit
25.00 – 125.00	mmol/24 Hour

24 Hour Urine Sodium

The kidney is central to the regulation and conservation of electrolytes in the body. Urinary sodium (Na+) excretion varies with dietary intake, and there is a large diurnal variation with the rate of Na+ excretion during the night being only 20% of the peak rate during the day. Urine sodium testing is used on the evaluation of acid-base abnormalities, water balance, water intoxication, and dehydration.

Source: Clinical Chemistry: Principles, Techniques, and Correlations by Bishop, Fody, and Schoeff

TEST DETAILS
MLLI CODE	J24UNA

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Ion-selective electrode diluted (Indirect)
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
24 hour urine	10 mL	17	Storage: 2 to 8˚C Stability: 45 days Storage: 20 to 25˚C Stability: 45 days Storage: -20˚C Stability: 1 year	During the start of collection, empty the bladder and discard the first urine output. Collect all the succeeding urine voided in a 24-hour period. Keep the urine container either in a refrigerator or in an ice chest.
NOTE	•If aliquoted sample, please indicate total volume in mL and specific gravity, date and time of start and end of collection

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
40 to 220	mmol/24 Hour

24 Hour Urine Urea Nitrogen

The urea nitrogen urine test measures the amount of urea nitrogen in a sample of urine collected over 24 hours (24-hour urine test test). Measurements obtained by this test are used in the diagnosis of renal and metabolic disease.

Source: Urea assay package insert

TEST DETAILS
MLLI CODE	J24UAC

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Urease
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
24 hour urine	10 mL	17	Storage: 2 to 8˚C Stability: 3 days Storage: 20 to 25˚C Stability: 3 days Storage: -20˚C Stability: 1 month	During the start of collection, empty the bladder and discard the first urine output. Collect all the succeeding urine voided in a 24-hour period. Keep the urine container either in a refrigerator or in an ice chest.
NOTE	•If aliquoted sample, please indicate total volume in mL and specific gravity, date and time of start and end of collection.

Conventional Reference Range	Conventional Unit
12.04 to 19.88	g/24 Hour
International Reference Range	International Unit
430.00 to 710.00	mmol/24 Hour

24 Hour Urine Uric Acid

This test is used in the assessment and management of patients with uric acid kidney stones.

Source: mauocliniclabs.com

TEST DETAILS
MLLI CODE	J24UA

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Uricase
Synonyms	Not Applicable
Acronyms	UA 24-hours Urine- Uric Acid 24-hours Urine

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
24 hour urine	10 mL	17	Storage: 2 to 8˚C Stability: 2 days Storage: 20˚C to 25˚C Stability: 2 days	During the start of collection, empty the bladder and discard the first urine output. Collect all the succeeding urine voided in a 24-hour period. Keep the urine container either in a refrigerator or in an ice chest.
NOTE	•If aliquoted sample, please indicate total volume in mL and specific gravity, date and time of start and end of collection.

Conventional Reference Range	Conventional Unit
250.85 – 750.84	mg/24 Hr
International Reference Range	International Unit
1.48 – 4.43	mmoL/24 Hr

5 HIAA Serotonin Quantity

5-hydroxyindoleacetic acid (5-HIAA) is an end-product of the trytophan metabolism and It is excreted in urine. It is formed as a result of deamination from serotonin. Serotonin, a powerful smooth muscle stimulant, is produced in large amounts by carcinoid tumors.

Source: Package Insert

TEST DETAILS
MLLI CODE	J5HSQN

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch Run	Wednesday Cut off: 07:00 am	Thursday 08:00 am

Assay Information
Methodology	Microcolumn chromatography
Synonyms	Not Applicable
Acronyms	5-HIAA - 5-HYDROXYINDOLEACETIC ACID

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
24 hour urine	10 mL	17	Storage: 2 to 8˚C Stability: 15 days Storage: -20˚C Stability: 1 month	3-4 days before sample collection, avoid eating of bananas, pineapples, avocados, kiwi fruits, red plums, tomatoes, walnuts, and chocolates.
NOTE	•If aliquoted sample, please indicate total volume in mL and specific gravity,date and time of start and end of collection. •Specimen must be collected in amber colored urine container. • *UNAVAILABLE AS OF FEBRUARY 2021

Conventional Reference Range	Conventional Unit
10.4 – 31.2	mg/24-hour
International Reference Range	International Unit
2 – 6	umol/24-hour

Acid Fast Bacilli Concentration

Acid fast stains are used to differentiate acid fast organisms such as mycobacteria. Detection of acid-fast bacilli (AFB) in stained and acid-washed smears examined microscopically may provide the initial bacteriologic evidence of the presence of mycobacteria in a clinical specimen. This test uses Kinyoun method of staining.

Source: Microbiology and Molecular Diagnosis in Pathology, 2017; Bailey and Scott's Diagnostic Microbiology

TEST DETAILS
MLLI CODE	JMBAFB

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily 2:00 p.m - 7:00 p.m	Same day after 6 hours

Assay Information
Methodology	Microscopic Identification
Synonyms	Acid Fast Bacilli Smear Acid Fast Stain
Acronyms	AFB- Acid Fast Bacilli

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Sputum Urine Aspirates Tissues Urine,Stool Other sterile body fluids/BAL	Urine: 60 mL Stool: Pea size Other samples:3 to 5 mL	16	Storage: 2 to 8˚C Stability: 7 days	No patient preparation
NOTE	•For sputum sample, preferably early morning for 2 consecutive days or spot testing, as requested by Attending physician. •For Urine samples-at least 60ml first morning specimen in a sterile container. Other samples- no preparation needed •Please indicate Time and Date of Collection •Swabs are not acceptable.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

Acid Fast Bacilli Smear/Direct

Acid fast stains are used to differentiate acid fast organisms such mycobacteria. Acid fast bacteria will be red, while nonacid fast bacteria will stain blue/green with the counterstain with the Kinyoun stain. Ziehl Nielson can also be used to stain mycobacteria but uses heat while the Kinyoun method does not. Procedure used technique that directly inoculated sample to slide with a specific smearing pattern and criterias.

Source: Microbiology and Molecular Diagnosis in Pathology, 2017; Bailey and Scott's Diagnostic Microbiology

TEST DETAILS
MLLI CODE	JAFBSD

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	CSF and BMA Daily 2: 00 p.m to 7:00 p.m Sputum DSSM Monday to Friday Cut off time: 3:00 p.m. Non-DSSM: 7:00 p.m	Same day after 6 hours

Assay Information
Methodology	Microscopic Identification
Synonyms	Direct Sputum Smear Microscopy
Acronyms	AFB- Acid Fast Bacilli DSSM- Direct Sputum Smear Microscopy

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
CSF and Bone Marrow Aspirate Sputum for DSSM	CSF & BMA 0.5 mL to 2 mL Sputum 3 mL to 5 mL	17	Storage: 2 to 8°C Stability: 24 hours	No patient preparation
NOTE	•No receiving of DSSM samples on weekends, unless 1st sample was submitted on a Friday. SPECIMEN RECEIVED BEYOND 3PM (DSSM) WILL BE PROCESSED THE FOLLOWING DAY . • All primary specimen containers must be labelled with at least two patient-specific identifiers. This is inclusive of patient name, date of birth, hospital number, unique other number, accession number. For specimens were site of origin is critical to analysis, it must be clearly identified on the container. Sputum Via Induction is not acceptable

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

Alanine Aminotransferase

Alanine Aminotransferase (ALT) is an enzyme involved in amino acid metabolism. It is found in many tissues, but the highest levels are found in the liver and kidney. ALT is used in the diagnosis and monitoring of liver disease associated with hepatic necrosis.

Source: Alanine Aminotransferase assay package insert

TEST DETAILS
MLLI CODE	JALTA

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	IFCC- International Federation of Clinical Chemistry
Synonyms	SGPT- Serum glutamic pyruvic transaminase
Acronyms	ALT- Alanine Aminotransferase SGPT- Serum glutamic pyruvic transaminase

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days Storage: 30˚C Stability: 3 days Storage: -40˚C Stability: 60 days	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
5.00 to 55.00	U/L

Albumin

Albumin is the most abundant protein in human serum. Elevated levels are usually the result of dehydration whereas decresed levles are found in variety of conditons including kidney disease, liver disease malabsorption, malnutrition, severe burns, infections and cancer.

Source: Albumin assay package insert

TEST DETAILS
MLLI CODE	JALBA

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Bromcresol green
Synonyms	Not Applicable
Acronyms	ALB- Albumin

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days Storage: 20 to 25˚C Stability: 7 days Storage: -20˚C Stability: 3 months	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
Less than 4 days : 2.80 to 4.40 5 days to 14 years: 3.80 to 5.40 15 to 60 years: 3.50 to 5.00 61 to 90 years: 3.20 to 4.60 Greater than 90 years old: 2.90 to 4.50	g/dL
International Reference Range	International Unit
Less than 4 days : 28.0 to 44.0 5 days to 14 years old: 38.0 to 54.0 15 to 60 years old: 35.0 to 50.0 61 to 90 years old: 32.0 to 46.0 Greater than 90 years old: 29.0 to 45.0	g/L

Albumin - Other Body Fluids

The Albumin-OBF test assist in identifying the cause of ascites. It aids in differentiating exudative and transudative pleural effusions.

Source: mayocliniclabs.com

TEST DETAILS
MLLI CODE	JALBBF

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Bromcresol green
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Body fluids: Peritoneal Fluid Pleural Fluid Synovial Fluid Drain Fluid	2 mL	17	Storage: 20-24 ˚C Stability: 24 hours Storage: 2-8 ˚C Stability: 7 days preferred. Storage: ≤ -20 ˚C Stability: 30 days	No patient preparation
NOTE	•It is recommended that freshly collected body fluid specimen be submitted in the laboratory as soon as possible. However, if delay in transportation occurs, it is vital to follow the suggested storage and stability.

Conventional Reference Range	Conventional Unit
No defined reference range	g/dL
International Reference Range	International Unit
Not Applicable	Not Applicable

Alkaline Phosphatase

The Alkaline Phosphatase assay is used for the quantitation of alkaline phosphatase in human serum. Hepatobiliary and bone diseases are the most common pathological inidcators of increased Alkaline Phosphatase.

Source: Alkaline Phosphatase assay package insert

TEST DETAILS
MLLI CODE	JAALK

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Para-nitrophenyl Phosphate
Synonyms	Not Applicable
Acronyms	ALP- Alkaline Phosphatase

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days Storage 20 to 25˚C Stability: 7 days Storage -20˚C Stability: 2 months	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
Less than 12 years old: Less than 500.00 Greater than 12 to 15 years old: Less than 750.00 Greater than 15 years old: 40.00 to 150.00	U/L
International Reference Range	International Unit
Less than 12 years old: Less than 500.00 Greater than 12 to 15 years old: Less than 750.00 Greater than 15 years old: 40.00 to 150.00	U/L

Alkaline Phosphatase Heat Fractionation

The Alkaline Phosphatase assay is used for the quantitation of alkaline phosphatase in human serum. Alkaline Phosphatase and Isoenzymes assist in the diagnosis of liver cancer and cirrhosis, or bone cancer and bone fracture.

Source: AFP assay package insert

TEST DETAILS
MLLI CODE	JAPHF

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Para-nitrophenyl Phosphate
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days Storage: 20 to 25˚C Stability: 7 days Storage: -20˚C Stability: 2 months	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
Greater than 25% – Hepatic Less than 25% – Osteoblastic	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

Allergen IgE - Dermatophagoides farinae

Specific IgE provides an objective measurement of the circulating IgE antibodies and the sensitization to a specific allergen. Specific IgE antibodies appear as a result of exposure and following sensitization to an allergen.

Source: ThermoFisher Scientific Product Catalogue 2020

TEST DETAILS
MLLI CODE	JAD2

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Tuesday and Friday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	FEIA- Fluoroenzyme Immunoassay Method
Synonyms	Not Applicable
Acronyms	D.Farinae- Dermatophagoides farinae

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7days	No patient preparation
NOTE	•Please check with Immunology Section for the availability of the allergen.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Undetectable: Less than 0.1	kUa/L

Allergen IgE - Dermatophagoides pteronyssinus / House Dust

Specific IgE provides an objective measurement of the circulating IgE antibodies and the sensitization to a specific allergen. Specific IgE antibodies appear as a result of exposure and following sensitization to an allergen.

Source: ThermoFisher Scientific Product Catalogue 2020

TEST DETAILS
MLLI CODE	JAD1

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Tuesday and Friday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	FEIA- Fluoroenzyme Immunoassay Method
Synonyms	Not Applicable
Acronyms	D.pteronyssinus- Dermatophagoides pteronyssinus

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7days	No patient preparation
NOTE	•Please check with Immunology Section for the availability of the allergen. Please indicate specific species of house dust or dust mite.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Undetectable: Less than 0.1	kUa/L

Allergen IgE - Almond

Specific IgE provides an objective measurement of the circulating IgE antibodies and the sensitization to a specific allergen. Specific IgE antibodies appear as a result of exposure and following sensitization to an allergen.

Source: ThermoFisher Scientific Product Catalogue 2020

TEST DETAILS
MLLI CODE	JAF20

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Tuesday and Friday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	FEIA- Fluoroenzyme Immunoassay Method
Synonyms	Not Applicable
Acronyms	IgE- Immunoglobulin E

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days	No patient preparation
NOTE	•Please check with Immunology Section for the availability of the allergen.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Undetectable: Less than 0.1	kUa/L

Allergen IgE - Beef

Specific IgE provides an objective measurement of the circulating IgE antibodies and the sensitization to a specific allergen. Specific IgE antibodies appear as a result of exposure and following sensitization to an allergen.

Source: ThermoFisher Scientific Product Catalogue 2020

TEST DETAILS
MLLI CODE	JAF27

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Tuesday and Friday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	FEIA- Fluoroenzyme Immunoassay Method
Synonyms	Not Applicable
Acronyms	IgE- Immunoglobulin E

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days	No patient preparation
NOTE	•Please check with Immunology Section for the availability of the allergen.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Undetectable: Less than 0.1	kUa/L

Allergen IgE - Bermuda Grass

Specific IgE provides an objective measurement of the circulating IgE antibodies and the sensitization to a specific allergen. Specific IgE antibodies appear as a result of exposure and following sensitization to an allergen.

Source: ThermoFisher Scientific Product Catalogue 2020

TEST DETAILS
MLLI CODE	JAG2

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Tuesday and Friday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	FEIA- Fluoroenzyme Immunoassay Method
Synonyms	Not Applicable
Acronyms	IgE- Immunoglobulin E

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days	No patient preparation
NOTE	•Please check with Immunology Section for the availability of the allergen

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Undetectable: Less than 0.1	kUa/L

Allergen IgE - Cheddar Cheese

Specific IgE provides an objective measurement of the circulating IgE antibodies and the sensitization to a specific allergen. Specific IgE antibodies appear as a result of exposure and following sensitization to an allergen.

Source: Thermo Fisher Scientific Product Catalogue 2020

TEST DETAILS
MLLI CODE	JAF81

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Tuesday and Friday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	FEIA- Fluoroenzyme Immunoassay Method
Synonyms	Not Applicable
Acronyms	IgE- Immunoglobulin E

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days	No patient preparation
NOTE	•Please check with Immunology Section for the availability of the allergen.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Undetectable: Less than 0.1	kUa/L

Allergen IgE - Chicken

Specific IgE provides an objective measurement of the circulating IgE antibodies and the sensitization to a specific allergen. Specific IgE antibodies appear as a result of exposure and following sensitization to an allergen.

Source: Thermo Fisher Scientific Product Catalogue 2020

TEST DETAILS
MLLI CODE	JAF83

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Tuesday and Friday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	FEIA- Fluoroenzyme Immunoassay Method
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days	No patient preparation
NOTE	•Please check with Immunology Section for the availability of the allergen.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Undetectable: Less than 0.1	kUa/L

Allergen IgE - Cockroach

Specific IgE provides an objective measurement of the circulating IgE antibodies and the sensitization to a specific allergen. Specific IgE antibodies appear as a result of exposure and following sensitization to an allergen.

Source: ThermoFisher Scientific Product Catalogue 2020

TEST DETAILS
MLLI CODE	JA15

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Tuesday and Friday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	FEIA- Fluoroenzyme Immunoassay Method
Synonyms	Not Applicable
Acronyms	IgE- Immunoglobulin E

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7days	No patient preparation
NOTE	•Please check with Immunology Section for the availability of the allergen.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Undetectable: Less than 0.1	kUa/L

Allergen IgE - Dog Dander

Specific IgE provides an objective measurement of the circulating IgE antibodies and the sensitization to a specific allergen. Specific IgE antibodies appear as a result of exposure and following sensitization to an allergen.

Source: ThermoFisher Scientific Product Catalogue 2020

TEST DETAILS
MLLI CODE	JAE2

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Tuesday and Friday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	FEIA- Fluoroenzyme Immunoassay Method
Synonyms	Not Applicable
Acronyms	IgE- Immunoglobulin E

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7days	No patient preparation
NOTE	•Please check with Immunology Section for the availability of the allergen.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Undetectable: Less than 0.1	kUa/L

Allergen IgE - Egg White

Specific IgE provides an objective measurement of the circulating IgE antibodies and the sensitization to a specific allergen. Specific IgE antibodies appear as a result of exposure and following sensitization to an allergen.

Source: ThermoFisher Scientific Product Catalogue 2020

TEST DETAILS
MLLI CODE	JAF1

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Tuesday and Friday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	FEIA- Fluoroenzyme Immunoassay Method
Synonyms	Not Applicable
Acronyms	IgE- Immunoglobulin E

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days	No patient preparation
NOTE	•Please check with Immunology Section for the availability of the allergen.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Undetectable: Less than 0.1	kUa/L

Allergen IgE - Egg Yolk

Specific IgE provides an objective measurement of the circulating IgE antibodies and the sensitization to a specific allergen. Specific IgE antibodies appear as a result of exposure and following sensitization to an allergen.

Source: ThermoFisher Scientific Product Catalogue 2020

TEST DETAILS
MLLI CODE	JAF75

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Tuesday and Friday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	FEIA- Fluoroenzyme Immunoassay Method
Synonyms	Not Applicable
Acronyms	IgE- Immunoglobulin E

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days	No patient preparation
NOTE	•Please check with Immunology Section for the availability of the allergen.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Undetectable: Less than 0.1	kUa/L

Allergen IgE - Fish Cod

Specific IgE provides an objective measurement of the circulating IgE antibodies and the sensitization to a specific allergen. Specific IgE antibodies appear as a result of exposure and following sensitization to an allergen.

Source: ThermoFisher Scientific Product Catalogue 2020

TEST DETAILS
MLLI CODE	JAF3

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Tuesday and Friday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	FEIA- Fluoroenzyme Immunoassay Method
Synonyms	Not Applicable
Acronyms	IgE- Immunoglobulin E

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7days	No patient preparation
NOTE	•Please check with Immunology Section for the availability of the allergen.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Undetectable: Less than 0.1	kUa/L

Allergen IgE - General food mix ( Egg White, Milk Fish, Wheat, Peanut, Soya)

Specific IgE provides an objective measurement of the circulating IgE antibodies and the sensitization to a specific allergen. Specific IgE antibodies appear as a result of exposure and following sensitization to an allergen.

Source: ThermoFisher Scientific Product Catalogue 2020

TEST DETAILS
MLLI CODE	JFX5

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Tuesday and Friday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	FEIA- Fluoroenzyme Immunoassay Method
Synonyms	Not Applicable
Acronyms	IgE- Immunoglobulin E

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7days	No patient preparation
NOTE	•Please check with Immunology Section for the availability of the allergen.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Negative	Not Applicable

Allergen IgE - Milk

Specific IgE provides an objective measurement of the circulating IgE antibodies and the sensitization to a specific allergen. Specific IgE antibodies appear as a result of exposure and following sensitization to an allergen.

Source: ThermoFisher Scientific Product Catalogue 2020

TEST DETAILS
MLLI CODE	JAF2

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Tuesday and Friday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	FEIA- Fluoroenzyme Immunoassay Method
Synonyms	Not Applicable
Acronyms	IgE- Immunoglobulin E

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days	No patient preparation
NOTE	•Please check with Immunology Section for the availability of the allergen.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Undetectable: Less than 0.1	kUa/L

Allergen IgE - Mold mix

Specific IgE provides an objective measurement of the circulating IgE antibodies and the sensitization to a specific allergen. Specific IgE antibodies appear as a result of exposure and following sensitization to an allergen.

Source: ThermoFisher Scientific Product Catalogue 2020

TEST DETAILS
MLLI CODE	JAMX2

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Tuesday and Friday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	FEIA- Fluoroenzyme Immunoassay Method
Synonyms	Not Applicable
Acronyms	IgE- Immunoglobulin E

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days	No patient preparation
NOTE	•Please check with Immunology Section for the availability of the allergen.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Negative	Not Applicable

Allergen IgE - Orange

Specific IgE provides an objective measurement of the circulating IgE antibodies and the sensitization to a specific allergen. Specific IgE antibodies appear as a result of exposure and following sensitization to an allergen.

Source: ThermoFisher Scientific Product Catalogue 2020

TEST DETAILS
MLLI CODE	JAF33

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Tuesday and Friday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	FEIA- Fluoroenzyme Immunoassay Method
Synonyms	Not Applicable
Acronyms	IgE- Immunoglobulin E

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days	No patient preparation
NOTE	•Please check with Immunology Section for the availability of the allergen.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Undetectable: Less than 0.1	kUa/L

Allergen IgE - Peanut

Specific IgE provides an objective measurement of the circulating IgE antibodies and the sensitization to a specific allergen. Specific IgE antibodies appear as a result of exposure and following sensitization to an allergen.

Source: ThermoFisher Scientific Product Catalogue 2020

TEST DETAILS
MLLI CODE	JAF13

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Tuesday and Friday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	FEIA- Fluoroenzyme Immunoassay Method
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days	No patient preparation
NOTE	•Please check with Immunology Section for the availability of the allergen.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Undetectable: Less than 0.1	kUa/L

Allergen IgE - Phadiatop (Molds, House dust mites, Cat epithelium, Bermuda grass, Pigweed)

Specific IgE provides an objective measurement of the circulating IgE antibodies and the sensitization to a specific allergen. Specific IgE antibodies appear as a result of exposure and following sensitization to an allergen.

Source: ThermoFisher Scientific Product Catalogue 2020

TEST DETAILS
MLLI CODE	JAPHA

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Tuesday and Friday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	FEIA- Fluoroenzyme Immunoassay Method
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days	No patient preparation
NOTE	•Please check with Immunology Section for the availability of the allergen.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Negative	Not Applicable

Allergen IgE - Pork

Specific IgE provides an objective measurement of the circulating IgE antibodies and the sensitization to a specific allergen. Specific IgE antibodies appear as a result of exposure and following sensitization to an allergen.

Source: ThermoFisher Scientific Product Catalogue 2020

TEST DETAILS
MLLI CODE	JAF26

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Tuesday and Friday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	FEIA- Fluoroenzyme Immunoassay Method
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days	No patient preparation
NOTE	•Please check with Immunology Section for the availability of the allergen.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Undetectable: Less than 0.1	kUa/L

Allergen IgE - Salmon

Specific IgE provides an objective measurement of the circulating IgE antibodies and the sensitization to a specific allergen. Specific IgE antibodies appear as a result of exposure and following sensitization to an allergen.

Source: ThermoFisher Scientific Product Catalogue 2020

TEST DETAILS
MLLI CODE	JAF41

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Tuesday and Friday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	FEIA- Fluoroenzyme Immunoassay Method
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days	No patient preparation
NOTE	•Please check with Immunology Section for the availability of the allergen.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Undetectable: Less than 0.1	kUa/L

Allergen IgE - Shrimps

Specific IgE provides an objective measurement of the circulating IgE antibodies and the sensitization to a specific allergen. Specific IgE antibodies appear as a result of exposure and following sensitization to an allergen.

Source: ThermoFisher Scientific Product Catalogue 2020

TEST DETAILS
MLLI CODE	JAF24

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Tuesday and Friday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	FEIA- Fluoroenzyme Immunoassay Method
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days	No patient preparation
NOTE	•Please check with Immunology Section for the availability of the allergen.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Undetectable: Less than 0.1	kUa/L

Allergen IgE - Soya Beans

Specific IgE provides an objective measurement of the circulating IgE antibodies and the sensitization to a specific allergen. Specific IgE antibodies appear as a result of exposure and following sensitization to an allergen.

Source: ThermoFisher Scientific Product Catalogue 2020

TEST DETAILS
MLLI CODE	JAF14

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Tuesday and Friday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	FEIA- Fluoroenzyme Immunoassay Method
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days	No patient preparation
NOTE	•Please check with Immunology Section for the availability of the allergen.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Undetectable: Less than 0.1	kUa/L

Allergen IgE - Squid

Specific IgE provides an objective measurement of the circulating IgE antibodies and the sensitization to a specific allergen. Specific IgE antibodies appear as a result of exposure and following sensitization to an allergen.

Source: ThermoFisher Scientific Product Catalogue 2020

TEST DETAILS
MLLI CODE	JAF58

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Tuesday and Friday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	FEIA- Fluoroenzyme Immunoassay Method
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days	No patient preparation
NOTE	•Please check with Immunology Section for the availability of the allergen.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Undetectable: Less than 0.1	kUa/L

Allergen IgE - Tuna

Specific IgE provides an objective measurement of the circulating IgE antibodies and the sensitization to a specific allergen. Specific IgE antibodies appear as a result of exposure and following sensitization to an allergen.

Source: ThermoFisher Scientific Product Catalogue 2020

TEST DETAILS
MLLI CODE	JAF40

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Tuesday and Friday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	FEIA- Fluoroenzyme Immunoassay Method
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days	No patient preparation
NOTE	•Please check with Immunology Section for the availability of the allergen.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Undetectable: Less than 0.1	kUa/L

Allergen IgE - Wheat

Specific IgE provides an objective measurement of the circulating IgE antibodies and the sensitization to a specific allergen. Specific IgE antibodies appear as a result of exposure and following sensitization to an allergen.

Source: ThermoFisher Scientific Product Catalogue 2020

TEST DETAILS
MLLI CODE	JAF4

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Tuesday and Friday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	FEIA- Fluoroenzyme Immunoassay Method
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days	No patient preparation
NOTE	•Please check with Immunology Section for the availability of the allergen.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Undetectable: Less than 0.1	kUa/L

Alpha Feto Protein

Alpha-fetoprotein (AFP) is a human tumor-associated protien. It has been shown that elevated values found in healthy individuals occurs in several malignant diseases, most notably nonseminomatous testicular cancer and primary hepatocellular cacinoma.

Source: AFP assay package insert

TEST DETAILS
MLLI CODE	JAFPA

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	CMIA-Chemiluminescent microparticle immunoassay
Synonyms	Not Applicable
Acronyms	AFP- Alpha Feto Protein

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: Room Temperature Stability: 3 days Storage 2-8 ˚C Stability: 7 days Storage: -20˚ C Stability: Greater than 7 days	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
0.90 to 8.83	ng/mL
International Reference Range	International Unit
0.74 to 7.30	IU/mL

Alpha Globin Genotyping

This assay is used for the identification of α-globin gene mutations; reduced or absent α-globin synthesis, mainly caused by deletions of one or both α-globin genes (α1,α2) and less frequently by point mutations, leads to α-thalassemia.

Source: www.viennalab.com/products/genetic-disorders/thalassemia

TEST DETAILS
MLLI CODE	JALPHA

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Wednesday Cut off Tuesday 1 :00 p.m	Friday (Received before Cut-off) Following Friday (Received after cut off)

Assay Information
Methodology	PCR- Polymerase Chain Reaction
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Whole blood	4 mL	5	Storage: 2 to 8°C Stability: 3 days	No patient preparation
NOTE	Requirements: 1. CBC Result 2. Hemoglobin Electrophoresis result

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

Amylase

Amylase is produced in the pancreas and parotid glands, normal individual have low but measurable serum amylase. Elevated result may be diagnosed for pancreatitis and other pancreatic disorders.

Source: Amylase assay package insert

TEST DETAILS
MLLI CODE	JAMYA

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	2-chloro-4-nitrophenyl-α-D-maltotrioside (CNPG3 Substrate)
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days Storage: 20-25˚C Stability: 24 hours Storage: -20˚C Stability: 3 months	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
Less than 14 days : 3.00 to 10.00 15 days to 12 weeks: 2.00 to 22.00 13 weeks to 11 months: 3.00 to 50.00 1 to 18 years old: 25.00 – 101.00 Greater than 19 years old: 28.00 – 100.00	U/L
International Reference Range	International Unit
Less than 14 days : 3.00 to 10.00 15 days to 12 weeks: 2.00 to 22.00 13 weeks to 11 months: 3.00 to 50.00 1 to 18 years old: 25.00 – 101.00 Greater than 19 years old: 28.00 – 100.00	U/L

Amylase - Other Body Fluids

The Amylase-OBF assay is used for the quantification of amylase in body fluid specimens. Body fluid amylase activity may become elevated due to the presence of pancreatitis, esophageal rupture, or amylase producing neoplasms.

Source: mayocliniclabs.com

TEST DETAILS
MLLI CODE	JAMYBF

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	2-chloro-4-nitrophenyl-α-D-maltotrioside (CNPG3 Substrate)
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Body fluids: •Peritoneal fluid •Pleural fluid •Pericardial fluid •Amniotic fluid •Drain fluid	2 mL	17	Storage: 20-24 ˚C Stability: 24 hours Storage: 2-8 ˚C Stability: 7 days preferred Storage:≤ -20 ˚C Stability: 30 days	No patient preparation
NOTE	•It is recommended that freshly collected body fluid specimen be submitted in the laboratory as soon as possible. However, if delay in transportation occurs, it is vital to follow the suggested storage and stability.

Conventional Reference Range	Conventional Unit
No defined reference range	U/L
International Reference Range	International Unit
Not Applicable	Not Applicable

ANA Profile (Lupus Panel)

This package test aids in the detection and diagnosis of certain autoimmune diseases such as lupus and Sjogren syndrome. ANA Profile includes Anti Nuclear Antibody (ANA) and double stranded DNA (dsDNA) test using indirect immunofluorescence method. Anti Smith, Anti RNP-70, Anti Jo-1, Anti SSA and Anti SSB are tested by using Enzyme Linked Immunosorbent Assay (ELISA).

Source: Package inserts

TEST DETAILS
MLLI CODE	JLEPRO

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Monday and Thursday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	ELISA- Enzyme Linked Immunosorbent Assay IIFT- Indirect Immunofluorescence Test
Synonyms	Lupus Erythematosus Profile - LE Profile Lupus Erythematosus Panel- LE Panel
Acronyms	LEPRO

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	3 mL	1 or 2	Storage: 2 to 8˚C Stability: 14 days	No patient preparation
NOTE	•Clinical abstract/initial diagnosis of the patient (if available)

Conventional Reference Range	Conventional Unit
ANA: Negative dSDNA: Negative Anti Smith: Negative:Less than 15U/mL Equivocal:15 to 25U/mL Positive: Greater than 25U/mL Anti RNP: Negative: Less than 25 U/mL Positive: Equal or Greater than 25 U/mL Anti JO-1: Negative:Less than 15U/mL Equivocal:15 to 25U/mL Positive: Greater than 25U/mL Anti SSA: Negative:Less than 15U/mL Equivocal:15 to 25 U/mL Positive: Greater than 25 U/mL Anti-SSB: Negative:Less than 15U/mL Equivocal:15 to 25 U/mL Positive: Greater than 25 U/mL	ANA and dsDNA: Not applicable Sm, RNP, JO-1, SSA, SSB: U/mL
International Reference Range	International Unit
Not Applicable	Not Applicable

Anti Cardiolipin IgG

This assay contributes to the diagnosis of antiphospholipid syndrome (APS). The quantitative determination of anti-cardiolipin IgG is very useful for monitoring SLE patients with secondary APS.

Source: Anti Cardiolipin IgG package insert

TEST DETAILS
MLLI CODE	JACAGu

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Daily Cut-off: 12:00 noon	Following day

Assay Information
Methodology	ELISA- Enzyme Linked Immunosorbent Assay
Synonyms	Anti Phospholipid IgG Anti Cardio (ACA) IgG
Acronyms	ACA- Anti Cardiolipin Antibodies IgG- Immunoglobulin G

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 5 days; Storage: -20˚C Stability: 6 months	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Negative: Less than 10 U/ml Positive: Equal or Greater than 10 U/ml	U/mL

Anti Cardiolipin IgM

This assay contributes to the diagnosis of antiphospholipid syndrome (APS). The quantitative determination of anti-cardiolipin IgM is very useful for monitoring SLE patients with secondary APS.

Source: Anti Cardiolipin IgM Package Insert

TEST DETAILS
MLLI CODE	JACAMu

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Daily Cut-off: 12:00 noon	Following day

Assay Information
Methodology	ELISA- Enzyme Linked Immunosorbent Assay
Synonyms	Anti Phospholipid IgM Anti Cardio (ACA) IgM
Acronyms	ACA- Anti Cardiolipin Antibodies IgM- Immunoglobulin M

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 5 days Storage: -20˚C Stability: 6 months	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Negative: Less than 7 U/ml Positive: Equal or Greater than 7 U/ml	U/mL

Anti - Cyclic Citrullinated Peptide

Citrulline is a non-standard amino acid, as it is not incorporated into proteins synthesis. Cyclic citrullinated peptide were equally specific for RA, but with a higher sensitivity with linear peptides. Detection of anti-CCP antibodies is used as an aid in the diagnosis of Rheumatoid Arthritis (RA).

Source: Anti-CCP assay package insert

TEST DETAILS
MLLI CODE	JCCPA

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	CMIA-Chemiluminescent microparticle immunoassay
Synonyms	Not Applicable
Acronyms	ANTI-CCP- Anti- Cyclic Citrullinated Peptide

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: Room Temperature Stability: Less than or equal to 22 hours Storage: 2 to 8˚ C Stability: Less than or equal to 7 days ,br> Storage: -20 ˚C Stability: Greater than 7 days	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
Negative: less than 5.0 Positive: greater than 5.0	U/mL
International Reference Range	International Unit
Non-Reactive: Less than 0.999 Reactive: Greater than 1.0	U/mL

Anti Double Stranded DNA

Anti-double stranded DNA antibody (anti-dsDNA) is one of a group of autoantibodies called antinuclear antibodies (ANA). Normally, antibodies protect against infection, but autoantibodies are produced when a person's immune system fails to adequately distinguish between "self" and "non-self." They mistakenly attack the body's own healthy cells, causing tissue and organ damage.

Source: IIFT: Crithidia luciliae sensitive (anti-dsDNA) package insert

TEST DETAILS
MLLI CODE	JNDNA

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Monday and Thursday Cut-off 8:00 a.m	Following day

Assay Information
Methodology	IIFT- Indirect Immunofluorescence
Synonyms	Antibody to ds-DNA Native double-stranded DNA Antibody Anti-DNA Double stranded DNA Antibody
Acronyms	ds-DNA - Double Stranded DeoxyriboNucleic Acid

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 14 days	No patient preparation
NOTE	•Clinical Abstract/Initial Diagnosis of patient (if available).

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Negative	Not Applicable

Anti Hepatitis A Virus Immunoglobulin G

Anti-HAV IgG implies past infection with hepatitis A virus (HAV) or vaccination against HAV.

Source: Anti-HAV IgG assay package insert

TEST DETAILS
MLLI CODE	JAIGG2

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	CMIA-Chemiluminescent microparticle immunoassay
Synonyms	Immunoglobulin G Antibody to Hepatitis A
Acronyms	HAV- Hepatitis A Virus IgG- Immunoglobulin G

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8 ⁰C Stability: Less than or equal to 14 days Storage: -10 ⁰C or colder Stability: Greater than 14 days	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
Nonreactive: Less than 1.0 Reactive : Greater than or equal to 1.0	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

Anti Hepatitis A Virus Immunoglobulin M

Hepatitis A is a self-limiting disease and is often a subclinical disorder. During the acute phase of HAV infection, IgM anti-HAV appears in the pateint's serum and is nearly always detectable at the onset of symptoms. In most cases, IgM anti-HAV response usually peaks within the first month of illness and can persist for up to six months.

Source: Anti-HAV IgM assay package insert

TEST DETAILS
MLLI CODE	JHIGM

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	CMIA-Chemiluminescent microparticle immunoassay
Synonyms	IGM Antibody to Hepatitis A Virus
Acronyms	HAV- Anti Hepatitis A Virus IgM- Immunoglobulin M

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8 ⁰C Stability: Less than or equal to 7 days Storage: -10˚ C or colder Stability: Greater than 7 days	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Nonreactive: Less than 1.0 Reactive: Greater than or equal to 1.0	Not Applicable

Anti Hepatitis B Core Immunoglobulin M

Viral specific IgM antibody has been detected in most acute viral infections and is a reliable marker of acute disease. The concentrations of anti-HBc IgM rise rapidly in patients with acute infection; high levels of anti-HBc IgM have been detected in patients with acute hepatitis B viral infection.

Source: Anti-HBc IgM assay package insert

TEST DETAILS
MLLI CODE	JAHIGM

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	CMIA-Chemiluminescent microparticle immunoassay
Synonyms	IgM antibody to Hepatitis B core antigen
Acronyms	ANTI-HBc IGM- Anti Hepatitis B Core Immunoglobulin M

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: ≤7 days Storage: -20˚C or colder Stability: >7 days	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
Nonreactive: Less than 1.0 Reactive : Greater than or equal to 1.0	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

Anti Hepatitis B Envelope

Anti-HBe is found in association with hepatitis B viral infection. Seroconversion from HBeAg to anti-HBe during acute hepatitis B infection is usually indicative of resolution of infection and a reduced level of infectivity.

Source: Anti-HBe assay package insert

TEST DETAILS
MLLI CODE	JHBEAB

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	CMIA-Chemiluminescent microparticle immunoassay
Synonyms	Antibody to Hepatitis B envelope antigen
Acronyms	Anti-Hbe- Anti Hepatitis B Envelope

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: Room Temperature Stability: ≤3 days Storage: 2 to 8˚C Stability: ≤7 days Storage: -20˚C or colder Stability: >7 days	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Nonreactive: Less than 1.0 Reactive: Greater than or equal to 1.0	Not Applicable

Anti Hepatitis B Surface

Anti-HBs are often used to monitor the success of Hepatitis B vaccination. The presence of anti-HBs has been shown to be important in protection against Hepatitis B virus (HBV) infection. Anti-HBs are also used to monitor the convalescence and recovery of Hepatitis B infected individuals.

Source: Anti-HBs assay package insert

TEST DETAILS
MLLI CODE	JANHBS

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	CMIA-Chemiluminescent microparticle immunoassay
Synonyms	Antibody to Hepatitis B surface Antigen
Acronyms	Anti-HBS- Anti Hepatitis B Surface

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 14 days Storage: -20˚C or colder Stability: >14 days	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Nonreactive: Less than 10.0 Reactive: Greater than or equal to 10.0	IU/L

Anti Hepatitis C Virus

The presence of Anti-HCV indicates that an individual may have been infected with HCV, may harbor infecious HCV, and/or may be capable of transmitting infection. HCV infection may develop into chronic hepatitis, cirrhosis, and/or increased risk of hepatocellular carcinoma.

Source: Anti-HCV assay package insert

TEST DETAILS
MLLI CODE	JHCV

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	CMIA-Chemiluminescent microparticle immunoassay
Synonyms	Antibody to Hepatitis C Virus
Acronyms	ANTI-HCV- Anti Hepatitis C Virus

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚ C Stability: Less than or equal to 7 days Storage: -20 ˚C or colder Stability: Greater than 7 days	No patient preparation
NOTE	•Please indicate if patient is pregnant or non-pregnant

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Nonreactive: 0 to 0.899 Gray zone: 0.9 to Less than 1.0 Reactive: Greater than or equal to 1.0	Not Applicable

Anti Jo 1

The test is used as an aid in the differential diagnosis of autoimmune connective tissue diseases, especially polymyositis and dermatomyositis. In myositis patients, autoantibodies against the Jo-1 antigen may indicate anti-synthetase syndrome.

Source: Anti Jo 1 Package Insert

TEST DETAILS
MLLI CODE	JAJO1

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Daily Cut-off: 12:00 noon	Following day

Assay Information
Methodology	ELISA- Enzyme Linked Immunosorbent Assay
Synonyms	Antihistidyl transfer RNA [t-RNA] synthetase
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 5 days Storage: -20˚C Stability: 6 months	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Negative: Less than 15 Equivocal:15 to 25 Positive: Greater than 25	U/mL

Anti Mitochondrial Antibody

Antimitochondrial antibodies (AMA) are autoantibodies that are strongly associated with primary biliary cholangitis (PBC), formerly called primary biliary cirrhosis. This test detects AMA in the blood qualitatively.

Source: IIFT Mosaic Basic Profile 1 Package Insert

TEST DETAILS
MLLI CODE	JAMA

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Monday and Thursday Cut-off: 08:00 a.m	Following day

Assay Information
Methodology	IIFT- Indirect Immunofluorescence
Synonyms	AMA (Antimitochondrial Antibodies) Antibodies to Microtubule Associated Protein 2 Antimitochondrial Antibodies
Acronyms	AMA- Anti Mitochondrial Antibody

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 14 days	No patient preparation
NOTE	•Clinical abstract/initial diagnosis of the patient (if available)

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Negative	Not Applicable

Anti Mitochondrial Antibody Quantitative

Antimitochondrial antibodies (AMA) are autoantibodies that are strongly associated with primary biliary cholangitis (PBC), formerly called primary biliary cirrhosis. This test detects and measures the amount (titer) of AMA in the blood.

Source: IIFT Mosaic Basic Profile 1 Package Insert

TEST DETAILS
MLLI CODE	JAMAQ

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Monday and Thursday Cut-off: 08:00 a.m	Following day

Assay Information
Methodology	IIFT- Indirect Immunofluorescence
Synonyms	AMA (Antimitochondrial Antibodies) Antibodies to Microtubule Associated Protein 2 Antimitochondrial Antibodies Quantitative
Acronyms	AMA- Anti Mitochondrial Antibody

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 14 days	No patient preparation
NOTE	•Clinical diagnosis or initial diagnosis of the patient (if available) Titer is not reported if the result is negative

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Negative	Not Applicable

Anti Nuclear Antibody

The presence of ANA may be a marker of an autoimmune process and is associated with several autoimmune disorders but is most commonly seen with the autoimmune disorder systemic lupus erythematosus (SLE).

Source: IIFT Mosaic: Hep2/Liver (Monkey) Package Insert

TEST DETAILS
MLLI CODE	JANA

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Monday and Thursday Cut-off: 08:00 a.m	Following day

Assay Information
Methodology	IIFT- Indirect Immunofluorescence
Synonyms	ANA Screen Hep2
Acronyms	ANA- Anti Nuclear Antibody; Hep- Human Epithelial Cell

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 14 days	No patient preparation
NOTE	•Clinical abstract/initial diagnosis of the patient (if available) Titer and Pattern will be reported only if ANA (ANTI NUCLEAR ANTIBODY) result is POSITIVE

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Negative	Not Applicable

Anti Ribonucleoproteins

RNP-70, the 70 kDa protein of the U1-snRNP complex, is one of the extractable nuclear antigens (ENA). It is useful for the diagnosis of mixed connective tissue disease (MCTD, Sharp syndrome) and related autoimmune diseases.

Source: Anti-RNP 70 Package Insert

TEST DETAILS
MLLI CODE	JRNP

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Daily Cut-off: 12:00 noon	Following day

Assay Information
Methodology	ELISA- Enzyme Linked Immunosorbent Assay
Synonyms	Anti-snRNP70 U1-snRNP
Acronyms	Anti RNP- Anti Ribonucleoproteins

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 5 days Storage: -20˚C Stability: 6 months	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Negative: Less than 25 Positive: Equal or Greater than 25	U/mL

Anti-SARS-CoV-2 IgG

SARS‑CoV‑2 IgG assay is designed to detect immunoglobulin class G antibodies to the nucleocapsid protein of SARS‑CoV‑2 in serum and plasma from patients who are suspected/infected by coronovirus disease. This assay is used as an aid in the diagnosis of SARS‑CoV‑2 infection.

Source: Anti-SARS-CoV-2 IgG assay package insert

TEST DETAILS
MLLI CODE	JCOIGG

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily: cut off 1200H and 2300H	At 1600H and 0400H

Assay Information
Methodology	CMIA-Chemiluminescent microparticle immunoassay
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 15-25℃ Stability:2 days Storage: 2-8℃ Stability: 7 days	No patient preparation
NOTE	•If aliquoted sample, please indicate total volume in mL and specific gravity, date and time of start and end of collection. •Collect urine specimen with 10 mL hydrochloric acid as preservative. •Specimen must be collected in amber colored urine container.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
<1.4	COI

Anti-SARS-CoV-2 Total

SARS‑CoV‑2 is the causative agent of Coronavirus Disease 2019 (COVID‑19). This assay is intended as an aid in the determination of the immune reaction and detects antibody titers to SARS‑CoV‑2.

Source: Anti-SARS-CoV-2 package insert

TEST DETAILS
MLLI CODE	JCOTTL

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily: cut off 1200H and 2300H	At 1600H and 0400H

Assay Information
Methodology	ECLIA- Electrochemiluminecense immunoassay
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 15-25℃ Stability:3 days Storage: 2-8℃ Stability: 7 days Storage: -15 to -25℃ Stability:28 days	No patient preparation
NOTE	•If aliquoted sample, please indicate total volume in mL and specific gravity, date and time of start and end of collection. < br>•Collect urine specimen with 10 mL hydrochloric acid as preservative. •Specimen must be collected in amber colored urine container.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
<1.0	COI

Anti - Scl 70

Anti-Scl-70 is an ELISA-based, automated, in-vitro test system for the quantitative determination of IgG antibodies against Scl-70 (DNA topoisomerase I) in human serum. This test is also useful in the differential diagnosis of Raynaud’s phenomenon. Autoantibodies against topoisomerase I are also a prognostic marker for the further development of systemic sclerosis.

Source: Anti-Scl 70 Package Insert

TEST DETAILS
MLLI CODE	JBSCL

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Daily Cut-off: 12:00 noon	Following day

Assay Information
Methodology	ELISA- Enzyme Linked Immunosorbent Assay
Synonyms	Anti-topoisomerase I
Acronyms	Anti- Scl 70- Scleroderma Antibody

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 5 days Storage: -20˚C Stability: 6 months	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Negative: Less than 15 Equivocal: 15 to 25 Positive: Greater than 25	U/mL

Anti Sjogren's Syndrome A

Anti-SS-A is an ELISA-based, automated, in-vitro, test system for the quantitative determination of IgG antibodies against SS-A 60 and SS-A 52 in human serum. Autoantibodies against the two antigens SS-A 52 and SS-A 60 are predominantly found in cases of collagenosis, particularly Sjögren’s syndrome, and various forms of lupus erythematosus.

Source: Anti SS-A Package Insert

TEST DETAILS
MLLI CODE	JSSA

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Daily Cut-off: 12:00 noon	Following day

Assay Information
Methodology	ELISA- Enzyme Linked Immunosorbent Assay
Synonyms	Anti-Ro Anti-Sjogren's Syndrome Anti-SSA (Anti-Sjogren's Syndrome A) Autoantibodies to SSA (Ro) Ro (Anti-SSA) Ro Autoantibodies Sjogren's Syndrome SSA (Anti-SSA) SSA Autoantibodies
Acronyms	Anti SSA/RO- Anti Sjogren's Syndrome A/RO

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 5 days Storage: -20˚C Stability: 6 months	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Negative: Less than 15 Equivocal:15 to 25 Positive: Greater than 25	U/mL

Anti Sjogren's Syndrome B

Anti-SS-B is an ELISA-based test system for the quantitative measurement of IgG class autoantibodies against SS-B in human serum. Antibodies against SS-B are used for the differential diagnosis of systemic inflammatory autoimmune diseases.

Source: Anti-SS-B Package Insert

TEST DETAILS
MLLI CODE	JSSB

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Daily Cut-off: 12:00 noon	Following day

Assay Information
Methodology	ELISA- Enzyme Linked Immunosorbent Assay
Synonyms	Anti-La Anti-Sjogren's Syndrome Anti-SSB (Anti-Sjogren's Syndrome B) Autoantibodies to SS-B/LA, Serum La (Anti-SSB) Sjogren's Syndrome SSB (Anti-SSB) SSB Autoantibodies
Acronyms	Anti SSB/LA: Anti Sjogren's Syndrome B/LA

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 5 days Storage: -20˚C Stability: 6 months	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Negative: Less than 15 Equivocal:15 to 25 Positive: Greater than 25	U/mL

Anti Smith

The detection of autoantibodies against Sm proteins is one of the ACR criteria for the diagnosis of systemic lupus erythematosus (SLE). Anti Smith antibodies serves as a prognostic marker for SLE.

Source: Anti Smith Package Insert

TEST DETAILS
MLLI CODE	JASM

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Daily Cut-off: 12:00 noon	Following day

Assay Information
Methodology	ELISA- Enzyme Linked Immunosorbent Assay
Synonyms	Not Applicable
Acronyms	Anti SM- Anti Smith

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 5 days Storage: -20˚C Stability: 6 months	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Negative: Less than 15 Equivocal:15 to 25 Positive: Greater than 25	U/mL

Anti Smooth Muscle Antibody

Smooth muscle antibodies (SMA) are autoantibodies, proteins produced by the body's immune system that recognize and attack its own actin, a protein found in smooth muscle and other tissues, especially the liver. This test detects and measures SMA (or antibody against actin) in the blood qualitatively.

Source: IIFT Mosaic Basic Profile 1 Package Insert

TEST DETAILS
MLLI CODE	JASMA

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Daily Cut-off: 12:00 noon	Following day

Assay Information
Methodology	IIFT- Indirect Immunofluorescence
Synonyms	Not Applicable
Acronyms	ASMA- Anti Smooth Muscle Antibody

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 14 days	No patient preparation
NOTE	•Clinical abstract/initial diagnosis of the patient (if available)

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Negative	Not Applicable

Anti Smooth Muscle Antibody Quantitative

Smooth muscle antibodies (SMA) are autoantibodies, proteins produced by the body's immune system that recognize and attack its own actin, a protein found in smooth muscle and other tissues, especially the liver. This test detects and measures the amount (titer) of SMA (or antibody against actin) in the blood.

Source: IIFT Mosaic Basic Profile 1 Package Insert

TEST DETAILS
MLLI CODE	JASMAQ

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Daily Cut-off: 12:00 noon	Following day

Assay Information
Methodology	IFF- Indirect Immunofluorescene
Synonyms	Not Applicable
Acronyms	ASMA- Anti Smooth Muscle Antibody

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 14 days	No patient preparation
NOTE	•Clinical abstract/initial diagnosis of the patient (if available) Titer is not reported if the result is negative.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Negative	Not Applicable

Anti - Streptolysin O

The group A β-hemolytic streptococci produce various toxins that can act as antigens. One of these exotoxins is streptolysin-O. The affected organism produces specific antibodies against the exotoxins, among which concentration of antistreptolysin-O in the patient's serum will enable to establish the degree of infection due to the β-hemolytic streptococcus.

Source: ASO assay package insert

TEST DETAILS
MLLI CODE	JASOA

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Immunoturbidimetric
Synonyms	ASO Titer
Acronyms	ASO- Anti- Streptolysin O

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 2 days Storage: -20˚C Stability: >2 days	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
Less than 200	IU/mL
International Reference Range	International Unit
Less than 200	IU/mL

Anti Thrombin III

Antithrombin III is the plasmatic inhibitor of thrombin and activated factor X and forms an irreversible inactive complex with these enzymes. This test aids in the quick determination of physiologically active AT III and allows the diagnosis of inherited and acquired antithrombin III deficiency, which represents an increased risk of thrombosis.

Source: Anti Thrombin III Package insert

TEST DETAILS
MLLI CODE	JAT3CS

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Wednesday Cut off 11:00 a.m	Within 24 hours

Assay Information
Methodology	Chromogenic Assay
Synonyms	Not Applicable
Acronyms	AT -Anti Thrombin

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Plasma	2 mL	10	Storage: 15 to 25 °C Stability: 6 hours Storage: 2 to 8°C Stability: 2 days Storage: - 20 Stability: 1 month	No patient preparation
NOTE	•Send sample within 4 hours from time of collection. For frozen samples, send within running day (one time thawing only).

Conventional Reference Range	Conventional Unit
75 to 125	%
International Reference Range	International Unit
75 to 125	%

Anti - Thyroglobulin

Thyroglobulin is a glycoprotein which is comprised of two identical subunits and represents the major protein found in thyroid. Anti-Tg are associated with cases of mild hypothyroidism or hyperthyroidism, and are frequently found in patients with other autoimmune diseases such as Rheumatoid Arthritis, Pernicious Anemia and Type I Diabetes.

Source: Anti-Tg assay package insert

TEST DETAILS
MLLI CODE	JTG

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	CMIA-Chemiluminescent microparticle immunoassay
Synonyms	Not Applicable
Acronyms	ANTI-TG- Anti - Thyroglobulin

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: Room Temperature Stability: ≤8 hours Storage: 2-8˚C Stability: ≤72 hours Storage: -10˚C or colder Stability: ≤30 days	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
Less than 4.11	IU/mL
International Reference Range	International Unit
Less than 4.11	IU/mL

Anti - Thyroid Peroxidase

TPO is a glycoprotein enzyme, in vivo function is the iodination of tyrosine in the synthesis of T3 and T4. Autoantibodies to TPO are potentially deleterious, and may have a pathogenic role in autoimmune thyroid disease. Anti-TPO antibodies are found often in conjunction with anti-Tg in the majority of cases of Hashimoto's tyroiditis, Primary Myxedema, and Grave's disease.

Source: Anti-TPO assay package insert

TEST DETAILS
MLLI CODE	JTPO

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	CMIA-Chemiluminescent microparticle immunoassay
Synonyms	Not Applicable
Acronyms	ANTI-TPO- 'Anti - Thyroid Peroxidase

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: Room Temperature Stability: Less than or equal to 8 hours Storage: 2 to 8˚ C Stability: Less than or equal to 72 hours Storage: -10˚ C or colder Stability: Less than or equal to 30 days	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
Greater than 5.61	IU/mL
International Reference Range	International Unit
Non-Reactive: Less than 0.80 Reactive: Greater than 1.2	IU/mL

APTS Test (Fetal Hemoglobin)

Grossly bloody stool and vomitus are sometimes seen in neonates as the result of swallowing maternal blood during delivery. The APT test helps to distinguish between the presence of fetal blood or maternal blood in an infant’s stool.

Source: Urinalysis and Body Fluids 5th Edition by Susan King Strasinger & Marjorie Schaub Di Lorenzo

TEST DETAILS
MLLI CODE	JAPTS

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Alkaline denaturation
Synonyms	Alkali Denaturation Test Apt-Downey Test
Acronyms	APT

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Grossly vomitus Stool or gastric fluid	0.5 mL to 1 mL	17	Storage: 18 to 24˚C Stability: 1 day	No patient preparation
NOTE	•Offered as in-house only. •This test is useful only on frankly bloody (red) stool or gastric specimens. Tarry (black) specimens are rejected because this would only indicate denatured hemoglobin.

Conventional Reference Range	Conventional Unit
Negative	Not Applicable
International Reference Range	International Unit
Negative	Not Applicable

Aspartate Aminotransferase

Aspartate Aminotransferase (AST) is one of a group of enzymes which catalyzes the interconversion of amino acids and alpha-keto acids. AST is mostly used in the evaluation of liver disease. Both AST and ALT are normally found in most body fluids, but not in urine except in instances of kidney lesions.

Source: Aspartate Aminotransferase assay package insert

TEST DETAILS
MLLI CODE	JASTA

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	NADH- Nicotinamide Adenine Dinucleotide (NAD) + Hydrogen (H)- (with P-5’-P) – IFCC
Synonyms	SGOT - Serum glutamic-oxaloacetic transaminase
Acronyms	AST - Aspartate Aminotransferase SGOT - Serum glutamic-oxaloacetic transaminase

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days Storage: 20 to 25˚C Stability: 4 days Storage: -20˚C Stability: 12 weeks	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
5.00 to 34.00	U/L

Bacterial Challenge

Bacteria challenge tests is performed to demonstrate that the product used on surfaces in manufacturing areas, hands, household, hospitality and commercial establishments, and other facilities are effective in the inactivation or removal of bacterial microorganisms.

Source: https://www.microbiologics.com; US Pharmacopeia. 2010. <1072>, Disinfectants and Antiseptics, Reissue USP33-NF28.

TEST DETAILS
MLLI CODE	JBACCH

Assay Timetable
Test Category	Test Schedule	Results Availability
Not Applicable	Not Applicable	2 to 4 Days

Assay Information
Methodology	Suspension Test
Synonyms	Disinfectant Qualification
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Disinfectants	> 10 mL	Disinfectants	Storage: Room Temperature Stability: 7 days	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

Bacterial Meningitis Antigen

This assay is an agglutination test intended for the rapid diagnosis of bacterial meningitis by the qualitative detection of soluble antigens to Neisseria meningitidis groups A, B/E. coli K1, C, Y/W 135, Haemophilus influenza type b, Streptococcus pneumonia and group B Streptococcus, in cerebrospinal fluid (CSF).

Source: Bacterial Meningitis Antigen Test Package Insert

TEST DETAILS
MLLI CODE	JPHADB

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Agglutination reaction
Synonyms	Phadebact Pastorex Meningitis
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
CSF	2 mL	17	Storage: 2 to 8˚C Stability: 4 hours	No patient preparation
NOTE	•If available, please provide patient's abstract/initial diagnosis for clinical interpretation. •Should be submitted to laboratory as soon as possible

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

BCR - ABL

BCR-ABL (QRT-PCR) is an automated test for quantifying the amount of BCR-ABL transcript as a ratio of BCRABL/ABL. The test utilizes automated, quantitative, real-time reverse transcription polymerase chain reaction (RT-qPCR).

Source: BCR-ABL Product Insert

TEST DETAILS
MLLI CODE	JBBQRT

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Monday to Friday Cut off 1:00 p.m	After 2 working days (Received before Cut-Off) After 3 working days (Received after Cut-Off)

Assay Information
Methodology	PCR-Polymerase Chain Reaction
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Whole blood	8 mL	5	Storage: 2 to 8°C Stability: 24 hours	No patient preparation
NOTE	•Freshly collected. Specimen MUST be processed within 24 hours after collection

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

Beta 2 - Microglobulin

β2-microglobulin is found on the surface of nearly all nucleated cells, where it constitutes the light chain of class I human leukocyte antigen (HLA). Serum levels of β2M are frequently elevated in patients with a variety of lymphoproliferative and inflammatory disorders reflecting an augmentationof synthesis.

Source: Beta 2-Microglobulin assay package insert

TEST DETAILS
MLLI CODE	JB2M

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Immunoturbidimetric
Synonyms	Not Applicable
Acronyms	B2M- Beta 2 - Microglobulin

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 8 days Storage: -20˚C Stability: >8 days	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
0.97 to 2.64	mg/L
International Reference Range	International Unit
Not Applicable	Not Applicable

Beta Crosslaps

This test is used for the in vitro quantitative determination of degradation products of type I collagen in human serum and plasma as an aid in assessing bone resorption. It aids in the monitoring of antiresorptive therapies in osteoporotic patients

Source: Beta Crosslaps package insert

TEST DETAILS
MLLI CODE	JBCL

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	ECLIA- Electrochemiluminecense Immunoassay
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 8 hours Storage: 20 to 25˚C Stability: 6 hours Storage: -20˚C Stability: 3 months	10-12 hours fasting
NOTE	•Please indicate date and time of last meal.

Conventional Reference Range	Conventional Unit
MALE: 30-50 y/o: < 0.584 51-70 y/o: < 0.704 > 71 y/o: < 0.854 FEMALE: Pre-menopausal:< 0.573 Post-menopausal:< 1.008	Not Applicable
International Reference Range	International Unit
Not Applicable	ng/mL

Beta Globin Genotyping

This assay is used for the identification of numerous defects in the β-globin gene, many of which cause structural abnormalities, such as HbS (sickle cell hemoglobin), HbC, HbE, or lead to impaired β-globin synthesis, known as β-thalassemia.

Source: www.viennalab.com/products/genetic-disorders/thalassemia

TEST DETAILS
MLLI CODE	JBETA

Assay Timetable
Test Category	Test Schedule	Results Availability
Batch	Thursday Cut off Tuesday 1 :00 p.m	Friday (Received before Cut-off) Following Friday (Received after cut off)

Assay Information
Methodology	PCR- Polymerase Chain Reaction
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Whole blood	4 mL	5	Storage: 2 to 8°C Stability: 3 days	No patient preparation
NOTE	•TEMPORARILY NOT AVAILABLE Requirements: 1. CBC Result 2. Hemoglobin Electrophoresis result

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

Bilirubin Profile

This package includes the following tests: Total Bilirubin, Direct Bilirubin, Indirect Bilirubin

Source: Package insert

TEST DETAILS
MLLI CODE	JBILIP

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Diazonium Salt, Colorimetric, Diazo Dye
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days Storage: 20 to 25˚C Stability: 2 days Storage: -20˚C Stability: 3 months	No patient preparation
NOTE	•Please refer to individual test item for more information on the specific assay in the package.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

Bleeding Time Macro

Bleeding time is a medical test that measures how fast small blood vessels in the skin stop bleeding. The duration of the bleeding from a standard puncture wound of the skin is a measure of the function of the platelets as well as the integrity of the vessel wall.

Source: Rodak’s Hematology- Clinical Principles, and Applications by E.M. Keohane, C.N. Otto, and J.M. Walenga

TEST DETAILS
MLLI CODE	JBT

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Duke's Method
Synonyms	BT (Bleeding Time)
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Capillary Blood	Not Applicable	Not Applicable	Not Applicable	No patient preparation
NOTE	•Offered as in-house only. •Elevated results are done at least twice. Requested for patients above 6 months old.

Conventional Reference Range	Conventional Unit
1 to 3	minutes and seconds
International Reference Range	International Unit
1 to 3	minutes and seconds

Bleeding Time Micro

Bleeding time is a medical test that measures how fast small blood vessels in the skin stop bleeding. The duration of the bleeding from a standard puncture wound of the skin is a measure of the function of the platelets as well as the integrity of the vessel wall.

Source: Rodak’s Hematology- Clinical Principles, and Applications by E.M. Keohane, C.N. Otto, and J.M. Walenga

TEST DETAILS
MLLI CODE	JBTM

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Duke's Method
Synonyms	BT (Bleeding Time)
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Capillary Blood	Not Applicable	Not Applicable	Not Applicable	No patient preparation
NOTE	•Offered as in-house only. •Elevated results are done at least twice. Requested for patients 0-6 months old.

Conventional Reference Range	Conventional Unit
1 to 3	minutes and seconds
International Reference Range	International Unit
1 to 3	minutes and seconds

Blood Alcohol Level

Determination of ethyl alcohol concentration is commonly used for measuring legal impairment, investigating forensic evidence, diagnosing and/or treating alcohol dependency, as well as detecting alcohol poisoning. Alcohol intoxication can lead to birth defects, loss of alertness, stupor, coma and death.

Source: Ethanol assay package insert

TEST DETAILS
MLLI CODE	JBLDAL

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Alcohol Dehydrogenase
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 6 months Storage: 20 to 25˚C Stability: 2 weeks Storage: -20˚C Stability: 6 months	No patient preparation
NOTE	•Collect via closed system; •If sample is to be transported, separate the serum from red blood cells via closed system; •Use povidone iodine as antiseptic. Do not use alcohol as antiseptic.

Conventional Reference Range	Conventional Unit
Greater than 50 mg/dL (mgs%): Euphoria and decreased inhibitions 100 to 300 mg/dL (mgs%) : Increased disorientation and incoordination Greater than 400 mg/dL (mgs%): Coma and death Reference: RA 10586	mg/dL (mgs%)
International Reference Range	International Unit
Not Applicable	Not Applicable

Blood Ammonia

Ammonia is derived from the catabolism of amino acids and from the action of intestinal bacteria on dietary protein, and is converted to urea in the liver hepatocytes and so rendered non-toxic. Elevated ammonia can have a toxic effect on the central nervous system, it may also be observed in severe liver failure, viral hepatitis or cirrhosis and it may occur with genetic defects of urea cycle and some other hereditary disorders.

Source: Ammonia assay package insert

TEST DETAILS
MLLI CODE	JMALDA

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Glutamate Dehydrogenase
Synonyms	Not Applicable
Acronyms	NH3- Ammonia

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Plasma	4 mL	5	Storage: 2 to 8˚C Stability: 2 hours Storage: -20˚C Stability: 3 weeks	No fasting, Patient is instructed to avoid any form of muscular exercises before and during blood extraction. Cigarette smoking (both patient and phlebotomy staff) prior to collection of the specimen is restricted.
NOTE	•Collection tube must be completely filled and immediately placed on ice. •Centrifuge the cold sample as quickly as possible and separate the plasma from blood cells using closed system. Rapid separation of plasma from blood cells is critical for obtaining reliable results. The standard recommendation is no more than 15 minutes from sample collection to the start of centrifugation. Timing is especially critical for patients with liver disease. Delays exceeding 15 minutes have been shown to increase ammonia concentration even at 0˚C. •Specimen obtained from House Call procedure is not acceptable unless otherwise, pre-analytical procedure stated above is strictly followed.

Conventional Reference Range	Conventional Unit
18.00 to 72.00	µmol/L
International Reference Range	International Unit
30.65 to 122.62	ug/dL

Blood Culture and Sensitivity Aerobic and Anaerobic

A blood culture is a laboratory test in which blood, taken from the patient, is inoculated into bottles containing culture media to determine whether infection-causing microorganisms (bacteria or fungi) are present in the patient’s bloodstream. Blood culture is the most widely used diagnostic tool for the detection of bacteremia and fungemia. It is the most important way to diagnose the etiology of bloodstream infections and sepsis and has major implications for the treatment of those patients.

Source: Adapted from ESCMID (European Society of Clinical Microbiology and Infectious Diseases) guidelines, 2012.7

TEST DETAILS
MLLI CODE	JMBBDC

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	If No growth: Preliminary report after 48 hours and Final report after 5 days if positive : Preliminary Report will be released 15 minutes after the Preliminary Gram Stain is validated. Refer to Bacteriology

Assay Information
Methodology	Colorimetric, Mass Spectrophotometry, Turbidimetric
Synonyms	Aerobic and Anaerobic Culture and Sensitivity
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Whole blood	8 mL - 10 mL	14 and 15	Room Temperature within 24 hours from the time of collection.	No patient preparation
NOTE	•Indications for Blood Culture are: Clinical features of sepsis including tachycardia, tachypnoea, increased or subnormal temperature and change in sensorium, hypotension or prostration. Suspicion of infective endocarditis. Pyrexia of unknown origin. Unexplained leukocytosis or leucopenia. Systemic and localized infections including suspected meningitis, osteomyelitis, septic arthritis, acute untreated bacterial pneumonia or other possible bacterial infection. Collect 2 sets of Blood Culture the least, but no more than 3 sets are generally required. Each set of blood cultures should be drawn from a separate site and inoculated into one aerobic and one anaerobic bottle Peripheral blood is the preferred sample site, if patient is with IV or port, 1 site should be extracted from the peripheral the second site will be from the port/IV. Follow aseptic technique in blood collection.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

Blood Culture and Sensitivity Pediatric

A blood culture is a laboratory test in which blood, taken from the pediatric patient, is inoculated into bottles containing culture media to determine whether infection-causing microorganisms (bacteria or fungi) are present in the patient’s bloodstream. Blood culture is the most widely used diagnostic tool for the detection of bacteremia and fungemia. It is the most important way to diagnose the etiology of bloodstream infections and sepsis and has major implications for the treatment of those pediatric patients.

Source: Adapted from ESCMID (European Society of Clinical Microbiology and Infectious Diseases) guidelines, 2012.7

TEST DETAILS
MLLI CODE	JBLDCA

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	If No growth: Preliminary report after 48 hours and Final report after 5 days if positive : Preliminary Report will be released 15 minutes after the Preliminary Gram Stain is validated. Refer to Bacteriology.

Assay Information
Methodology	Colorimetric,Mass Spectrophotometry, Turbidimetric
Synonyms	Aerobic Culture and Sensitivity
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Whole blood	1 to 3 mL	13	Room Temperature within 24 hours from the time of collection.	No patient preparation
NOTE	•Indications for Blood Culture are: Clinical features of sepsis including tachycardia, tachypnoea, increased or subnormal temperature and change in sensorium, hypotension or prostration; Suspicion of infective endocarditis; Pyrexia of unknown origin; Unexplained leukocytosis or leucopenia; Systemic and localized infections including suspected meningitis, osteomyelitis, septic arthritis, acute untreated bacterial pneumonia or other possible bacterial infection. Collect 2 sets of Blood Culture the least, but no more than 3 sets are generally required. Each set of blood cultures should be drawn from a separate site and inoculated into one aerobic and one anaerobic bottle Peripheral blood is the preferred sample site, if patient is with IV or port, 1 site should be extracted from the peripheral the second site will be from the port/IV. Follow aseptic technique in blood collection.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

Blood Urea Nitrogen

Measurements obtained by this test are used in the diagnosis of a certain renal and metabolic diseases. The determination of serum urea nitrogen is a widely used test for the evaluation of kidney function.

Source: Urea assay package insert

TEST DETAILS
MLLI CODE	JBUNA

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Urease
Synonyms	Not Applicable
Acronyms	BUN- Blood Urea NItrogen

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days Storage: 20 to 25˚C Stability: 24 hours	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
0 to 14 days : 2.80 to 22.96 15 days to 11 months : 3.36 to 16.80 1 to 9 years old : 8.96 to 22.12 Male – 10 to 18 years old : 7.28 to 19.09 Female 10 to 18 years old: 7.28 to 21.00 19 to 60 years old: 5.88 to 19.88 All 61 years old and above: 8.12 to 22.96	mg/dL
International Reference Range	International Unit
0 to 14 days: 1.00 to 8.20 15 days to 11 months: 1.20 to 6.00 1 to 9 years old: 3.20 to 7.90 Male – 10 to 18 years : 2.60 to 6.80 Female – 10 to 18 years : 2.60 to 7.50 19 to 60 years old : 2.10 – 7.10 61 years old and above: 2.90 – 8.20	mmol/L

Blood Urea Nitrogen

This test is for the quantitative determination of urea in blood from protein breakdown that provides information for metabolic status, for the evaluation of renal function and determination of end-stage renal failure and urea concentration in dialysis patients.

Source: Reflotron Urea package insert

TEST DETAILS
MLLI CODE	JERBUN

Assay Timetable
Test Category	Test Schedule	Results Availability
STAT	Daily	Within 20 minutes

Assay Information
Methodology	Reflectance Photometry
Synonyms	Not Applicable
Acronyms	BUN- Blood Urea Nitrogen

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Whole blood	2 mL	5 or 8	Storage: 15 to 25˚C Stability: 8 hours	No patient preparation
NOTE	•Offered to MMC ONLY.

Conventional Reference Range

Conventional Unit

Urea
Below 65 years: 19.20 to 50.00
Above 65 years: 19.20 to 71.00
Blood Urea Nitrogen Below 65 years: 9.33 to 23.25
Above 65 years: 9.33 to 33.33

mg/dL

International Reference Range

International Unit

Urea
Below 65 years: 3.33 to 8.30
Above 65 years: 3.33 to 11.90

Blood Urea Nitrogen
Below 65 years: 3.33 to 8.30
Above 65 years: 3.33 to 11.90

mmol/L

Brain Natriuretic Peptide

BNP is synthesized and released into the blood in response to volume overload or conditions that cause ventricular stretch. BNP plasma levels aids in the diagnosis of congestive heart failure.

Source: BNP assay package insert

TEST DETAILS
MLLI CODE	JBNP

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	CMIA-Chemiluminescent microparticle immunoassay
Synonyms	Not Applicable
Acronyms	BNP- Brain Natriuretic Peptide

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Plasma	4 mL	5	Storage: Room Temperature Stability: Test within 4 hours of collection Storage: 2-8˚C Stability: Test within 24 hours of collection Storage: -20˚C Stability: ≤3 months	No patient preparation
NOTE	•Collect specimen in plastic tubes only.

Conventional Reference Range

Conventional Unit

Male
0 to 44 years old: 0 to 73
Greater than 44 to 54 years old: 0 to 40
Greater than 54 to 64 years old: 0 to 80
Greater than 64 to 74 years old: 0 to 150
Greater than 74 years old: 0 to 121

Female
0 to 44 years old: 0 to 89
Greater than 44 to 54 years old: 0-111
Greater than 54 to 64 years old: 0 to 155
Greater than 64 to 74years old: 0 to 159
Greater than 74 years old: 0 to 266

pg/mL

International Reference Range

International Unit

Not Applicable

C Peptide

Connecting peptide (C-peptide) is a biologically inactive chain formed during the proteolytic conversion of proinsulin to insulin in the pancreatic beta cells. It is used as an aid in the diagnosis and treatment of patients with abnormal insulin secretion including diabetes mellitus.

Source: C-Peptide assay package insert

TEST DETAILS
MLLI CODE	JCPEPA

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	CMIA-Chemiluminescent microparticle immunoassay
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8 ˚C Stability: Less than or equal to 48 hours Storage: 15 to 30 ˚C Stability: Less than or equal to 24 hours Storage: -10˚ C or colder Stability: Greater than 48 hours	8-10 hours fasting
NOTE	None

Conventional Reference Range	Conventional Unit
Less than 5.19	ng/mL
International Reference Range	International Unit
Less than 1730.00	pmol/L

C3 Beta Complement

C3 Beta Complement is an acute phase reactant present in classical and alternate pathways producing tissue damage and inflammation. Elevated levels of C3 are associated with rheumatic disease, viral hepatitis, myocardial infarction, cancer, diabetes, pregnancy, sarcoidosis, amyloidosis, thyroiditis, inflammatory bowel disease, and pneumococcal pneumonia. Low levels of of C3 occur in individuals with congenital deficiency or immunologic diseases such as systemic lupus erythematosus (SLE).

Source: C3 Beta Complement assay package insert

TEST DETAILS
MLLI CODE	JC3BCA

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Immunoturbidimetric
Synonyms	Not Applicable
Acronyms	C3- Complement component 3

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 8 days Storage: -20˚C Stability: 8 days	No patient preparation
NOTE	•Transport under ice.

Conventional Reference Range

Conventional Unit

Male
0 to 14 years old: 0.080 to 0.170
Greater than 14 years old: 0.082 to 0.185

Female
0 to 14 years old: 0.082 to 0.173
Greater than 14 years old: 0.083 to 0.193

g/dL

International Reference Range

International Unit

Male
0 to 14 years old: 0.80 to 1.70
Greater than 14 years old: 0.82 to 1.85

Female
0 to 14 years old: 0.82 to 1.73
Greater than 14 years old: 0.83 to 1.93

g/L

C4 Beta Complement

C4 Beta Complement is an acute phase reactant and rise rapidly during inflammatory episodes. Increased C4 levels are associated with acute phase reactions and certain malignancies. Decreased levels are observed in Immune complex diseases, Hypergammaglobulinemic states, active SLE, and Hereditary angioedema.

Source: C4 Beta Complement assay package insert

TEST DETAILS
MLLI CODE	JC4BCA

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Immunoturbidimetric
Synonyms	Not Applicable
Acronyms	C4- Complement component 4

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 2 days	No patient preparation
NOTE	None

Conventional Reference Range

Conventional Unit

Male
0 to 14 years old: 0.014 to 0.044
Greater than 14 years old: 0.015 to 0.053

Female
0 to 14 years old: 0.013 to 0.046
Greater than 14 years old: 0.015 to 0.057

g/dL

International Reference Range

International Unit

‘Male
0 to 14 years old: 0.14 to 0.44
Greater than 14 years old: 0.15 to 0.53

Female
0 to 14 years old: 0.13 to 0.46
Greater than 14 years old: 0.15 to 0.57

g/L

CA 72-4

The tumor associated glycoprotein (TAG) 72, also known as CA 72-4 is a mucin protein of high molecular weight and found on the surface of many cancer cells, including stomach, ovary, breast, colon and pancreatic cells. Elevated serum levels are primarily found in gastric cancer patients, but can also be found in certain malignant diseases like pneumonia, pancreatitis, liver cirrhosis and ovarian cysts.

Source: Roche Elecsys CA 72-4 package insert

TEST DETAILS
MLLI CODE	JCA724

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	ECLIA- Electrochemiluminecense Immunoassay
Synonyms	TAG 72 (Tumor associatedglycoprotein 72)
Acronyms	CA 72-4 - Cancer Antigen 72-4 TAG 72- Tumor associatedglycoprotein 72

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 30 days Storage: 20 to 25˚C Stability: 1 day Storage: -20˚C Stability: 90 days	No patient preparation
NOTE	"*UNAVAILABLE AS OF FEBRUARY 2021. "

Conventional Reference Range	Conventional Unit
U/mL	N/A
International Reference Range	International Unit
	0-6.9

Calcium

Viral specific IgM antibody has been detected in most acute viral infections and is a reliable marker of acute disease. The concentrations of anti-HBc IgM rise rapidly in patients with acute infection; high levels of anti-HBc IgM have been detected in pat

Source: Linne & Ringsrud's Clinical Laboratory Science 6th Edition

TEST DETAILS
MLLI CODE	JCAA

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Arsenazo III complex
Synonyms	Not Applicable
Acronyms	CA - Calcium

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 3 weeks Storage: 20 to 25˚C Stability: 7 days Storage: -20˚C Stability: 8 months	No patient preparation
NOTE	None

Conventional Reference Range

Conventional Unit

Male
0 to 10 days old: 7.62 to 10.43
Greater than 10 to 2 years old: 9.02 to 11.03
Greater than 2 to 12 years old: 8.82 to 10.83
Greater than 12 to 60 years old: 8.42 to 10.23
Greater than 60 years old: 8.82 to 10.03

Female
0 to 10 days: 7.62 to 10.43
Greater than 10 to 2 years old: 9.02 to 11.03
Greater than 2 to 12 years old: 8.82 to 10.83
Greater than 12 to 60 years old: 8.42 to 10.23
Greater than 60 years old: 8.42 to 10.23

mg/dL

International Reference Range

International Unit

Male
0 to 10 days old: 1.90 to 2.60
Greater than 10 to 2 years old: 2.25 to 2.75
Greater than 2 to 12 years old: 2.20 to 2.70
Greater than 12 to 60 years old: 2.10 to 2.55
Greater than 60 years old: 2.20 to 2.50

Female
0 to 10 days: 1.90 to 2.60
Greater than 10 to 2 years old: 2.25 to 2.75
Greater than 2 to 12 years old: 2.20 to 2.70
Greater than 12 to 60 years old: 2.10 to 2.55
Greater than 60 years old: 2.10 to 2.55

mmol/L

Cancer Antigen 125

Measurement of Cancer Antigen 125 (CA 125) is useful for monitoring response to therapy with patients with epithelial ovarian cancer. Persistently rising CA 125 values may be associated with malignant disease and poor response to therapy. Decreasing values may indicate a favorable response to therapy.

Source: CA 125 assay package insert

TEST DETAILS
MLLI CODE	JCA125

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	CMIA-Chemiluminescent microparticle immunoassay
Synonyms	Not Applicable
Acronyms	CA 125- Cancer Antigen 125

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: Less than or equal to 7 days Storage: -20˚ C or colder Stability: Greater than 7 days	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
0 to 35	U/mL
International Reference Range	International Unit
Not Applicable	Not Applicable

Cancer Antigen 15-3

Cancer Antigen 15-3 (CA 15-3) is used as an aid in the management of Stage II and III breast cancer patients. Increasing and decreasing values of CA 15-3 correlates with disease progression and regression, respectively. Elevated values can also be seen in individuals with nonmalignant conditions such as cirrhosis, hepatitis, autoimmuno disorders, and benign disease of the ovary and breast.

Source: CA 15-3 assay package insert

TEST DETAILS
MLLI CODE	JCA15A

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	CMIA-Chemiluminescent microparticle immunoassay
Synonyms	Not Applicable
Acronyms	CA 15-3- Cancer Antigen 15-3

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: Less than or equal to 7 days Storage: -20˚ C or colder Stability: Greater than 7 days	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
0.00 to 31.30	U/mL
International Reference Range	International Unit
Not Applicable	Not Applicable

Cancer Antigen 19-9

Cancer Antigen 19-9 (CA 19-9) measurement is used as an aid in the management of pancreatic cancer patients. High CA 19-9 values have been observed in various gastrointestinal conditions, metastases, and cystic fibrosis.

Source: CA 19-9 assay package insert

TEST DETAILS
MLLI CODE	JCA19A

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	CMIA-Chemiluminescent microparticle immunoassay
Synonyms	Not Applicable
Acronyms	CA 19-9- Cancer Antigen 19-9

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: Less than or equal to 7 days Storage: -20˚ C or colder Stability: Greater than 7 days	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
0.00 to 37.00	U/mL
International Reference Range	International Unit
Not Applicable	Not Applicable

Carbamazepine

Carbamazepine is an anticonvulsant drug. It is used in the treatment of both generalized tonic-clonic and simple and complex partial seizures because of its inhibition of repetitive firing on neurons. Measurements obtained are used in monitoring to help ensure appropriate therapy.

Source: Carbamazepine assay package insert

TEST DETAILS
MLLI CODE	JCARBA

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	CMIA-Chemiluminescent microparticle immunoassay
Synonyms	Tegretol
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days Storage: 15 to 30˚C Stability: 24 hours Storage: -20˚C or colder Stability: greater than 7 days	No patient preparation
NOTE	•Indicate date and time of last dose, dosage and time of extraction.

Conventional Reference Range	Conventional Unit
Optimum therapeutic level: 4 to 12	µg/mL
International Reference Range	International Unit
Not Applicable	Not Applicable

Carbon Dioxide

Measurement of serum carbon dioxide total ( CO2 ) is necessary for the evaluation of acid-base status. High CO2 content may be observed in compensated respiratory acidosis and metabolic alkalosis. Low CO2 content may be observed in compensated respiratory alkalosis and metabolic acidosis.

Source:

TEST DETAILS
MLLI CODE	JCO2A

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Phospho (enol) pyruvate (PEP) Carboxylase
Synonyms	Not Applicable
Acronyms	CO2- Carbon Dioxide

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days Storage: 20 to 25˚C Stability: 1 day Storage: -20˚C Stability: 2 weeks	No patient preparation
NOTE	•It is recommended that specimens be assayed on the day of collection. •Aliquot specimen using closed system method.

Conventional Reference Range	Conventional Unit
0 to 1 years old: 13.00 to 22.00 Greater than 18 years old: 20.00 to 28.00 Greater than 18 to 60 years old: 22.00 to 29.00 Greater than 60 years old: 23.00 to 31.00	meq/L
International Reference Range	International Unit
0 to 1 years old: 13.00 to 22.00 Greater than 1 to 18 years old: 20.00 to 28.00 Greater than 18 to 60 years old: 22.00 to 29.00 Greater than 60 years old: 23.00 to 31.00	mmol/L

Carcinoembryonic Antigen

Measurement of Carcinoembryonic Antigen (CEA) is useful in the prognosis and management of cancer patients. Increased CEA values are observed in patients with digestive tract cancers, other nonmalignant and malignant disorders such as colorectal, gastric, breast, lung, prostatic, pancreatic, and ovarian carcinoma.

Source: CEA assay package insert

TEST DETAILS
MLLI CODE	JCEAA

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	CMIA-Chemiluminescent microparticle immunoassay
Synonyms	Not Applicable
Acronyms	CEA- Carcinoembryonic Antigen

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days Storage: -20˚C or colder Stability: Greater than 7 days	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
Less than 5.00	‘ng/mL
International Reference Range	International Unit
Not Applicable	Not Applicable

Cardiac Enzymes

"This test package is a biomarker for myocardial infarction. It includes the following tests: Aspartate Aminotransferase, Total CPK, CK-MB Isoenzyme, and Lactate Dehydrogenase."

Source: Package Inserts

TEST DETAILS
MLLI CODE	JCARDE

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Not Applicable
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2-8°C Stability: 72 hours	No patient preparation
NOTE	•Please refer to individual test item for more information on the specific assay in the package.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

Cell Count

Differential cell count is the most diagnostically significant test performed on body fluids. This test aids in the diagnosis of systemic disease, inflammation, malignancy and trauma.

Source: Urinalysis and Body fluids by Susan King Strasinger, Marjorie Schaub Di Lorenzo, 5th Edition

TEST DETAILS
MLLI CODE	JUCSF

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Microscopy
Synonyms	Body Fluid Cell count and Diff Count
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
•Cerebrospinal fluid •Peritoneal/Ascites •Pleural fluid •Synovial fluid •Pericardial fluid	2 mL	17	Optimal specimen: Storage: 2 to 8 ˚C Stability: 1 hour Specimen must be processed as soon as possible. If not, specimen must be stored at Storage: 2 to 8 ˚C Stability: 24 hours	No patient preparation
NOTE	•'It is recommended that freshly collected specimen be submitted in the laboratory as soon as possible. However, if delay in transportation occurs, it is vital to follow the updated storage and stability.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

Cerebrospinal Fluid Total Protein

CSF protein measurements are used in the diagnosis and treatment of conditions such as meningitis, brain tumors, and infections of the central nervous system.

Source: Urine/CSF Protein assay package insert

TEST DETAILS
MLLI CODE	JCSFPR

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Benzethonium chloride
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
CSF	2 mL	17	Storage: 2 to 8˚C Stability: 6 days Storage: 20 to 25˚C Stability: 24 hours Storage: -20˚C Stability: 1 year	Patient will undergo spinal tap procedure.
NOTE	•Always indicate collection tube number.

Conventional Reference Range	Conventional Unit
0 to 1 month old: 20.0 to 80.0 Greater than 1 month old and above: 15.0 to 45.0	mg/dL
International Reference Range	International Unit
0 to 1 month old: 200.0 to 800.0 Greater than 1 month old and above: 150.0 to 450.0	mg/L

Ceruloplasmin

Determination of ceruloplasmin level is useful in cases of central nervous system diseases. It aids in the diagnosis of Wilson’s disease, Menkes syndrome, and copper deficiency.

Source: Ceruloplasmin assay package insert

TEST DETAILS
MLLI CODE	JCERPA

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Turbidimetric/immunoturbidimetric
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 2 weeks Storage: 20 to 25˚C Stability: 8 days Storage: -20˚C Stability: 3 months	No patient preparation
NOTE	•Pls check with Laboratory Section concerned if further clarification is needed

Conventional Reference Range	Conventional Unit
20 to 60	mg/dL
International Reference Range	International Unit
0.20 to 0.60	g/L

CHEM 12

This package includes the following tests: Fasting Blood Glucose, Blood Urea Nitrogen , Sodium , Potassium, Chloride, Calcium, Carbon Dioxide, Total Protein, Albumin , Globulin, Aspartate aminotransferase, Alkaline phosphatase, and Total Bilirubin.

Source: Package Inserts

TEST DETAILS
MLLI CODE	JCH12A

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Not Applicable
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days Storage: 20 to 25˚C Stability: 2 days Storage: -20˚C Stability: 1 day	10 - 14 hours fasting
NOTE	•Please refer to individual test item for more information on the specific assay in the package. Indicate date and time of last meal.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

CHEM 15

This package includes the following tests:Fasting Blood Glucose, Blood Urea Nitrogen , Sodium , Potassium, Chloride, Uric Acid , Calcium , Carbon Dioxide, Cholesterol, Total Protein , Albumin, Globulin, Aspartate aminotransferase, Alkaline phosphatase, and Total Bilirubin.

Source: Package Inserts

TEST DETAILS
MLLI CODE	JCH15A

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Not Applicable
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days Storage: 20 to 25˚C Stability: 2 days Storage: -20˚C Stability: 1 day	10 - 14 hours fasting
NOTE	•Please refer to individual test item for more information on the specific assay in the package. Indicate date and time of last meal.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

CHEM 16

This package includes the following tests: Fasting Blood Glucose, Blood Urea Nitrogen, Sodium, Potassium, Chloride, Uric Acid, Calcium , Carbon Dioxide, Cholesterol, Total Protein , Albumin, Globulin, Aspartate aminotransferase, Alkaline phosphatase, and Total Bilirubin.

Source: Package Inserts

TEST DETAILS
MLLI CODE	JCH16A

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Not Applicable
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days Storage: 20 to 25˚C Stability: 2 days Storage: -20˚C Stability: 1 day	10 - 14 hours fasting
NOTE	•Please refer to individual test item for more information on the specific assay in the package. Indicate date and time of last meal.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

CHEM 17

This package includes the following tests: Sodium, Potassium, BUN, Fasting Blood Glucose, Cholesterol, Triglycerides, Uric Acid, SGOT, SGPT, Calcium, Phosphorus, Chloride, Alkaline Phosphatase, Total Bilirubin, Albumin, Globulin, Total Protein, LDH, and Total CPK.

Source: Package Inserts

TEST DETAILS
MLLI CODE	JCH17A

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Not Applicable
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days Storage: 20 to 25˚C Stability: 2 days Storage: -20˚C Stability: 1 day	12-14 hours fasting
NOTE	•Please refer to individual test item for more information on the specific assay in the package. Indicate date and time of last meal.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

CHEM 19

This package includes the following tests: Sodium, Potassium, Creatinine, BUN, Fasting Blood Glucose, Cholesterol, Triglycerides, Uric Acid, SGOT, SGPT, Calcium, Phosphorus, Chloride, Alkaline Phosphatase, Total Bilirubin, Albumin, Globulin, Total Protein, LDH, and Total CPK.

Source: Package Inserts

TEST DETAILS
MLLI CODE	JCH19A

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Not Applicable
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days Storage: 20 to 25˚C Stability: 2 days Storage: -20˚C Stability: 1 day	12-14 hours fasting
NOTE	•Please refer to individual test item for more information on the specific assay in the package. Indicate weight, date and time of last meal.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

CHEM 23

This package includes the following tests: Sodium, Potassium, Creatinine, BUN, Fasting Blood Glucose, Cholesterol, Triglycerides, HDL, LDL, Uric Acid, SGOT, SGPT, Calcium, Phosphorus, Chloride, Alkaline Phosphatase, Total Bilirubin, Albumin, Total Protein, Globulin, LDH, Total CPK, Carbon Dioxide, GGTP, and Amylase.

Source: Package Inserts

TEST DETAILS
MLLI CODE	JCH23A

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Not Applicable
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days Storage: 20 to 25˚C Stability: 2 days Storage: -20˚C Stability: 1 day	12-14 hours fasting
NOTE	•Please refer to individual test item for more information on the specific assay in the package. Indicate weight, date and time of last meal.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

CHEM Neuro

This package includes the following tests: Sodium, Potassium, Creatinine, BUN, Fasting Blood Glucose, Cholesterol, Triglycerides, Uric Acid, and SGPT.

Source: Package Inserts

TEST DETAILS
MLLI CODE	JCHENA

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Not Applicable
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days Storage: 20 to 25˚C Stability: 2 days Storage: -20˚C Stability: 1 day	12-14 hours fasting
NOTE	•Please refer to individual test item for more information on the specific assay in the package. Indicate weight, date and time of last meal.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

Chikungunya

This test is used in the detection of Chikungunya virus, that causes a disease syndrome characterized by fever, headache, rash, nausea, vomiting, myalgia and arthralgia and its transmission to human is mainly through Aedes species mosquitoes.

Source: Product insert.

TEST DETAILS
MLLI CODE	JCHKPC

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Monday to Friday Cut off 8:00 a.m	After 1 working day (Received before Cut-Off) After 2 working days (Received after Cut-Off)

Assay Information
Methodology	PCR- Polymerase Chain Reaction
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Whole blood Serum or Plasma	4 mL 2 mL	5 1 or 5	Whole blood Storage: 2 to 8°C Stability: 3 days Serum or Plasma Storage: -20°C Stability: 5 days	No patient preparation
NOTE	None

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

Chikungunya IgM

Chikungunya IgM test is a solid phase immunochromatographic assay for rapid qualitative detection of IgM antibodies to Chikungunya. Chikungunya fever is transmitted to humans by the bite of a variety of mosquitoes.

Source: Chikungunya IgM Package Insert

TEST DETAILS
MLLI CODE	JCHIKM

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	ICT-Immunochromatography
Synonyms	Chikungunya Antibody Test
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 3 days Storage: -20˚C Stability: 14 days	No patient preparation
NOTE	•Unavailable as of May 2020

Conventional Reference Range	Conventional Unit
Negative	Not Applicable
International Reference Range	International Unit
Negative	Not Applicable

Chlamydia Antigen

Chlamydia test is a solid phase immunochromatographic assay for the rapid, qualitative detection of Chlamydia antigen directly from endocervical swab and cytology brush specimens. Chlamydia trachomatis is a bacterium which causes a sexually transmitted infection.

Source: Chlamydia Antigen Test Package Insert

TEST DETAILS
MLLI CODE	JCHLAM

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	ICT-Immunochromatography
Synonyms	Chlamydiazyme
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Urethral/Endocervical swab (w/o any tinge of blood or mucus)	Not Applicable	24	Storage: 15 to 27˚C Stability: 6 hours Storage: 2 to 8˚C Stability: 3 days	No patient preparation
NOTE	•Only Polyester Swabs should be used. Please acquire swab from Immunology section. NO wooden swab will be accepted. Fresh specimens are recommended

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Negative	Not Applicable

Chlamydia trachomatis/ Neisseria gonorrhoeae (CT/NG) PCR

This test is used in the detection and differentiation of Chlamydia trachomatis from Neisseria gonorrhea to aid in the diagnosis of chlamydial and/or gonorrheal urogenital disease. Assay may be used to test the specimens from asymptomatic and symptomatic individuals both male and female.

Source: Xpert CT/NG Assay product insert

TEST DETAILS
MLLI CODE	JCT NG

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Monday to Friday Cut off 1:00 p.m	After 1 working day (Received before Cut-Off) After 2 working days (Received after Cut-Off)

Assay Information
Methodology	PCR- Polymerase Chain Reaction
Synonyms	Not Applicable
Acronyms	CT/NG - Chlamydia trachomatis/ Neisseria gonorrhoeae

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Urine Vaginal/Endocervical	10 mL 1 mL	17 23	Urine Storage: 2 to 8°C Stability: 3 days Vaginal/Endocervical. Storage: 2 to 8°C Stability: 2 weeks	No patient preparation
NOTE	Urine: First catch urine Vaginal/Endocervical: Dedicated collection container: Xpert CT/NG Collection Kit

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

Chloride

"Chloride is the major extracellular anion. It plays an important role in determining the osmotic pressure, which controls the distribution of water among cells, plasma, and interstitial fluid, and maintaining electrical neutrality. "

Source: Linne & Ringsrud's Clinical Laboratory Science 6th Edition

TEST DETAILS
MLLI CODE	JCLA

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Ion-selective electrode diluted indirect
Synonyms	Not Applicable
Acronyms	CL- Chloride

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Serum	2 mL	1 or 2	Storage: 2 to 8˚C Stability: 7 days Storage: 20 to 25˚C Stability: 7 days Storage: -20˚C Stability: 1 year	No patient preparation
NOTE	•To obtain optimal results, it is recommended to send specimen within 4 hours after specimen collection.

Conventional Reference Range	Conventional Unit
98.00 – 107.00	meq/L
International Reference Range	International Unit
98.00 – 107.00	mmol/L

Chloride - Other body fluids

Measurment of Chloride in body fluids other than blood can aid in the diagnosis of different diseases such as Cystic Fibrosis, Cirrhosis, and may be used for pancreatic function testing.

Source: aruplab.com/bodyfluids

TEST DETAILS
MLLI CODE	JCLOBF

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Ion-selective electrode diluted indirect
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Body Fluids: • Peritoneal fluid •Pleural fluid •Pericardial fluid •Amniotic fluid	2 mL	17	Storage: 20-24 ˚C Stability: 24 hours Storage: 2-8 ˚C Stability: 7 days Storage: ≤ -20 ˚C Stability:30 days	No patient preparation
NOTE	•It is recommended that freshly collected body fluid specimen be submitted in the laboratory as soon as possible. However, if delay in transportation occurs, it is vital to follow the suggested storage and stability.

Conventional Reference Range	Conventional Unit
Not Applicable	mmol/L
International Reference Range	International Unit
Not Applicable	Not Applicable

Cholesterol - Other body fluids

Measurement of Cholesterol in body fluids other than blood is useful in evaluation of different diseases such as cholesterol pericarditis, differentiation of exudates and transudates, and in distinguishing chylothorax from pseudochylothorax.

Source: aruplab.com/bodyfluids

TEST DETAILS
MLLI CODE	JCHLBF

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Enzymatic Chod- PAP
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Body fluids: •Peritoneal fluid •Pleural fluid •Pericardial fluid •Amniotic fluid •Dialysate fluid •Drain fluid	2 mL	17	Storage: 20-24 ˚C Stability: 24 hours Storage: 2-8˚C Stability: 7 days Storage: ≤ -20 ˚C Stability: 30 days preferred.	No patient preparation
NOTE	•It is recommended that freshly collected body fluid specimen be submitted in the laboratory as soon as possible. However, if delay in transportation occurs, it is vital to follow the suggested storage and stability.

Conventional Reference Range	Conventional Unit
Not Applicable	mg/dL
International Reference Range	International Unit
Not Applicable	Not Applicable

Clostridium difficile Antigen

Clostridium difficile GDH is a rapid qualitative enzyme immunoassay screening test to detect Clostridium difficile antigen, glutamate dehydrogenase, in fecal specimens from persons suspected of having C. difficile infection (CDI). This test does not distinguish between toxigenic and non-toxigenic strains of C. difficile

Source: Clostridium difficile Antigen Package Insert

TEST DETAILS
MLLI CODE	JCDEFF

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	EIA - Enzyme Immunoassay
Synonyms	Clostridium difficile GDH Antigen Test
Acronyms	C. Difficile - Clostridium Difficile C. Diff- Clostrodium Difficile

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Stool	Pea size	18	Storage: 2 to 8˚C Stability: 5 days Storage: -20˚C Stability: 30 days	No patient preparation
NOTE	•Fresh random stool in sterile bottle, should be submitted to the laboratory within 1 hour from collection. Should not be contaminated with urine, water or other contaminants

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

Clot Retraction

Clot retraction is the process of shrinking the formed clot (reducing its volume), mediated by contraction of the intracellular actin-myosin cytoskeleton of the activated platelets incorporated in the clot. This is done by incubating the specimen at 37 degrees Celsius for 1 hour.

Source: Clinical Diagnosis and Management by John Bernard Henry, M.D.

TEST DETAILS
MLLI CODE	JCRS

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4hours

Assay Information
Methodology	Clot Retraction Method
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Whole Blood	5 mL	2	Room Temperature	No patient preparation
NOTE	•Offered as in-house only. •Specimen must be transported to the section immediately (within 30 minutes from time of collection), and in an upright position (inverted). The date and time of collection must be noted in the tube.

Conventional Reference Range	Conventional Unit
20 to 65	%
International Reference Range	International Unit
20 to 65	%

Clotting Time (Lee and White Method)

Clotting time is used as a screening test to measure intrinsic coagulation system and to monitor heparin. Severe haemophilia, afibrinogenemia, and severe fibrinolytic states cause a prolonged clotting time, as do circulating anticoagulants (inhibitors).

Source: Brown, B.A. (1993). Hematology: Principles and Procedures. (6th ed.). Philadelphia: Lea & Febiger. Aster, R.

TEST DETAILS
MLLI CODE	JCT

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Clotting
Synonyms	Lee and White Method
Acronyms	CT- Clotting Time

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Whole Blood	5mL	2	Not applicable	No patient preparation
NOTE	Offered as in-house only. Freshly collected specimen only. Test done on-site

Conventional Reference Range	Conventional Unit
	5-15
International Reference Range	International Unit
minutes

Clotting Time (Slide Method)

Clotting time is used as a screening test to measure intrinsic coagulation system and to monitor heparin. Severe haemophilia, afibrinogenemia, and severe fibrinolytic states cause a prolonged clotting time, as do circulating anticoagulants (inhibitors).

Source: Brown, B.A. (1993). Hematology: Principles and Procedures. (6th ed.). Philadelphia: Lea & Febiger. Aster, R.

TEST DETAILS
MLLI CODE	JCTM

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	Clotting
Synonyms	Slide Method
Acronyms	CT- Clotting Time

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Whole Blood	1 drop	Slide	Not applicable	No patient preparation
NOTE	Offered as in-house only. Freshly collected specimen only. Test done on-site

Conventional Reference Range	Conventional Unit
	2-5
International Reference Range	International Unit
minutes

Cold Agglutinins

Cold agglutinin disease is an autoimmune disease characterized by the presence of high concentrations of circulating antibodies, usually IgM, directed against red blood cells. It is a form of autoimmune hemolytic anemia, specifically one in which antibodies only bind red blood cells at low body temperatures, typically 28-31

Source: Surhone, L., Tennoe, M., & Henssonow, S. (2010). Cold Agglutinin Disease. Betascript Publishing.

TEST DETAILS
MLLI CODE	JCOLDA

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Following day

Assay Information
Methodology	Agglutination reaction
Synonyms	Not Applicable
Acronyms	Not Applicable

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Whole Blood	5 mL	2	Storage: 2 to 8˚C Stability: 14 days	Pre warm tube at 37°C. Upon extraction, transport specimen immediately to the Laboratory at 37°C.
NOTE	•Offered in-house only, can't be sent out Specimen must be accompanied with doctor's request and patient's abstract/initial diagnosis for clinical interpretation if available. •Transport extracted specimen immediately. •Note exact date and time of extraction.

Conventional Reference Range	Conventional Unit
Not Applicable	Not Applicable
International Reference Range	International Unit
Not Applicable	Not Applicable

Complete Blood Count

A complete blood count (CBC) is performed on automated hematology profiling instruments and includes the RBC, WBC, and platelet measurements. It is a blood test used to evaluate the overall health and detect a wide range of disorders, including anemia, infection and leukemia.

Source: RODAK’s Hematology Clinical Principles and Applications 5th Edition

TEST DETAILS
MLLI CODE	JCBC

Assay Timetable
Test Category	Test Schedule	Results Availability
Routine	Daily	Within 4 hours

Assay Information
Methodology	RBC, Hct, and Platelet Count - Impedance Method with hydrodynamic focusing Hemoglobin - non-cyanide determination WBC and differential count - fluorescence flow cytometry (hydrodynamically focused)
Synonyms	Not Applicable
Acronyms	CBC- Complete Blood Count

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Whole blood	2 mL	5	Storage: 2 to 8˚C Stability: 24 hours	No patient preparation
NOTE	•Send sample within 4 hours from time of collection or store at 2 to 8˚C for 24 hours.

Conventional Reference Range

Conventional Unit

‘HEMOGLOBIN
0 to 1 day 135 to 225
2 to 7 days 135 to 225
8 to 29 days 100 to 215
1 to 5 months 100 to 180
6 to 11 months 95 to 135
1 to 5 years 105 to 135
6 to 11 years 115 to 135
12 to 17 years 115 to 135
18 years and above Female 123 to 153
18 years and above Male 140 to 165

HEMATOCRIT
0 to 1 day 0.42 to 0.67
2 to 7 days 0.42 to 0.67
8 to 29 days 0.31 to 0.66
1 to 5 months 0.31 to 0.55
6 to 11 months 0.29 to 0.41
1 to 5 years 0.33 to 0.39
6 to 11 years 0.34 to 0.40
12 to 17 years 0.35 to 0.45
18 years and above Female 0.359 to 0.446
18 years and above Male 0.415 to 0.490

RBC
0 to 1 day 3.9 to 6.6
2 to 7 days 3.9 to 6.6
8 to 29 days 3.0 to 6.3
1 to 5 months 3.0 to 5.4
6 to 11 months 3.1 to 4.5
1 to 5 years 3.4 to 5.4
6 to 11 years 3.9 to 5.3
12 to 17 years 4.6 to 5.2
18 years and above Female 4.5 to 5.1
18 years and above Male 4.5 to 5.9

WBC
0 to 1 day 9.0 to 34
2 to 7 days 5.0 to 34
8 to 29 days 5.0 to 21
1 to 5 months 5.0 to 19.5
6 to 11 months 6.0 to 17.5
1 to 5 years 6.0 to 17.5
6 to 11 years 5.0 to 14.5
12 to 17 years 4.5 to 13.5
18 years and above Female 4.4 to 11.0
18 years and above Male 4.4 to 11.0
HEMOGLOBIN
0 to 1 day 135 to 225
2 to 7 days 135 to 225
8 to 29 days 100 to 215
1 to 5 months 100 to 180
6 to 11 months 95 to 135
1 to 5 years 105 to 135
6 to 11 years 115 to 135
12 to 17 years 115 to 135
18 years and above Female 123 to 153
18 years and above Male 140 to 165

HEMATOCRIT
0 to 1 day 0.42 to 0.67
2 to 7 days 0.42 to 0.67
8 to 29 days 0.31 to 0.66
1 to 5 months 0.31 to 0.55
6 to 11 months 0.29 to 0.41
1 to 5 years 0.33 to 0.39
6 to 11 years 0.34 to 0.40
12 to 17 years 0.35 to 0.45
18 years and above Female 0.359 to 0.446
18 years and above Male 0.415 to 0.490

RBC
0 to 1 day 3.9 to 6.6
2 to 7 days 3.9 to 6.6
8 to 29 days 3.0 to 6.3
1 to 5 months 3.0 to 5.4
6 to 11 months 3.1 to 4.5
1 to 5 years 3.4 to 5.4
6 to 11 years 3.9 to 5.3
12 to 17 years 4.6 to 5.2
18 years and above Female 4.5 to 5.1
18 years and above Male 4.5 to 5.9

WBC
0 to 1 day 9.0 to 34
2 to 7 days 5.0 to 34
8 to 29 days 5.0 to 21
1 to 5 months 5.0 to 19.5
6 to 11 months 6.0 to 17.5
1 to 5 years 6.0 to 17.5
6 to 11 years 5.0 to 14.5
12 to 17 years 4.5 to 13.5
18 years and above Female 4.4 to 11.0
18 years and above Male 4.4 to 11.0

MCH
0 to 1 day 31 to 37
2 to 7 days 28 to 40
8 to 29 days 28 to 40
1 to 5 months 28 to 40
6 to 11 months 25 to 35
1 to 5 years 23 to 31
6 to 11 years 24 to 30
12 to 17 years 25 to 34
18 years and above 27.5 to 33.2

MCHC
0 to 1 day 0.29 to 0.37
2 to 7 days 0.28 to 0.38
8 to 29 days 0.28 to 0.38
1 to 5 months 0.29 to 0.37
6 to 11 months 0.30 to 0.36
1 to 5 years 0.30 to 0.36
6 to 11 years 0.31 to 0.37
12 to 17 years 0.31 to 0.37
18 years and above 0.334 to 0.355

MCV
0 to 1 day 95 to 121
2 to 7 days 88 to 126
8 to 29 days 85 to 126
1 to 5 months 85 to 123
6 to 11 months 74 to 108
1 to 5 years 70 to 86
6 to 11 years 75 to 87
12 to 17 years 77 to 95
18 years and above 80 to 96

NEUTROPHIL
0 to 1 day 33 to 86
2 to 7 days 30 to 61
8 to 29 days 30 to 47
1 to 5 months 20 to 46
6 to 11 months 16 to 48
1 to 5 years 13 to 55
6 to 11 years 30 to 55
12 to 17 years 40 to 59
18 years and above 40 to 70

STAB/BAND
0 to 1 day 0 to 9
2 to 7 days 0 to 9
8 to 29 days 0 to 7
1 to 5 months 0 to 6
6 to 11 months 0 to 6
1 to 5 years 0 to 6
6 to 11 years 0 to 6
12 to 17 years 0 to 7
18 years and above 0 to 6

LYMPHOCYTES
0 to 1 day 21 to 36
2 to 7 days 21 to 80
8 to 29 days 40 to 84
1 to 5 months 50 to 84
6 to 11 months 33 to 77
1 to 5 years 35 to 92
6 to 11 years 30 to 82
12 to 17 years 26 to 44
18 years and above 22 to 43

MONOCYTES
0 to 1 day 2 to 10
2 to 7 days 2 to 12
8 to 29 days 3 to 12
1 to 5 months 3 to 10
6 to 11 months 0 to 7
1 to 5 years 0 to 6
6 to 11 years 0 to 5
12 to 17 years 0 to 5
18 years and above 0 to 7

EOSINOPHIL
0 to 1 day 0 to 3
2 to 7 days 0 to 5
8 to 29 days 0 to 5
1 to 5 months 1 to 5
6 to 11 months 1 to 4
1 to 5 years 0 to 4
6 to 11 years 0 to 4
12 to 17 years 0 to 4
18 years and above 0 to 4

BASOPHIL
0 to 1 day 0 to 2
2 to 7 days 0 to 1
8 to 29 days 0 to 1
1 to 5 months 0 to 1
6 to 11 months 0 to 1
1 to 5 years 0 to 1
6 to 11 years 0 to 1
12 to 17 years 0 to 1
18 years and above 0 to 1

Hemoglobin: g/L
Hematocrit: –
RBC: x1012/L
WBC: x109/L
MCH: pg
MCHC: –
MCV: fL
Neutrophil: –
Stab/Band: –
Lymphocyte: –
Monocyte: –
Eosinophil: –
Basophil: –

International Reference Range

International Unit

‘HEMOGLOBIN
0 to 1 day 13.5 to 22.5
2 to 7 days 13.5 to 22.5
8 to 29 days 10.0 to 21.5
1 to 5 months 10.0 to 18.0
6 to 11 months 9.5 to 13.5
1 to 5 years 10.5 to 13.5
6 to 11 years 11.5 to 13.5
12 to 17 years 11.5 to 13.5
18 years and above Female 12.3 to 15.3
18 years and above Male 14.0 to 16.5

HEMATOCRIT
0 to 1 day 42 to 67
2 to 7 days 42 to 67
8 to 29 days 31 to 66
1 to 5 months 31 to 55
6 to 11 months 29 to 41
1 to 5 years 33 to 39
6 to 11 years 34 to 40
12 to 17 years 35 to 45
18 years and above Female 35.9 to 44.6
18 years and above Male 41.5 to 49.0

RBC
0 to 1 day: 3.9 to 6.6
2 to 7 days: 3.9 to 6.6
8 to 29 days: 3.0 to 6.3
1 to 5 months: 3.0 to 5.4
6 to 11 months: 3.1 to 4.5
1 to 5 years: 3.4 to 5.4
6 to 11 years: 3.9 to 5.3
12 to 17 years: 4.6 to 5.2
18 years and above Female: 4.5 to 5.1
18 years and above Male: 4.5 to 5.9

WBC
0 to 1 day 9.0 to 34
2 to 7 days 5.0 to 34
8 to 29 days 5.0 to 21
1 to 5 months 5.0 to 19.5
6 to 11 months 6.0 to 17.5
1 to 5 years 6.0 to 17.5
6 to 11 years 5.0 to 14.5
12 to 17 years 4.5 to 13.5
18 years and above Female 4.4 to 11.0
18 years and above Male 4.4 to 11.0

MCH
0 to 1 day 31 to 37
2 to 7 days 28 to 40
8 to 29 days 28 to 40
1 to 5 months 28 to 40
6 to 11 months 25 to 35
1 to 5 years 23 to 31
6 to 11 years 24 to 30
12 to 17 years 25 to 34
18 years and above 27.5 to 33.2

MCHC
0 to 1 day 29 to 37
2 to 7 days 28 to 38
8 to 29 days 28 to 38
1 to 5 months 29 to 37
6 to 11 months 30 to 36
1 to 5 years 30 to 36
6 to 11 years 31 to 37
12 to 17 years 31 to 37
18 years and above 33.4 to 35.5

MCV
0 to 1 day 95 to 121
2 to 7 days 88 to 126
8 to 29 days 85 to 126
1 to 5 months 85 to 123
6 to 11 months 74 to 108
1 to 5 years 70 to 86
6 to 11 years 75 to 87
12 to 17 years 77 to 95
18 years and above 80 to 96

NEUTROPHIL
0 to 1 day 33 to 86
2 to 7 days 30 to 61
8 to 29 days 30 to 47
1 to 5 months 20 to 46
6 to 11 months 16 to 48
1 to 5 years 13 to 55
6 to 11 years 30 to 55
12 to 17 years 40 to 59
18 years and above 40 to 70

STAB/BAND
0 to 1 day 0 to 9
2 to 7 days 0 to 9
8 to 29 days 0 to 7
1 to 5 months 0 to 6
6 to 11 months 0 to 6
1 to 5 years 0 to 6
6 to 11 years 0 to 6
12 to 17 years 0 to 7
18 years and above 0 to 6

LYMPHOCYTES
0 to 1 day 21 to 36
2 to 7 days 21 to 80
8 to 29 days 40 to 84
1 to 5 months 50 to 84
6 to 11 months 33 to 77
1 to 5 years 35 to 92
6 to 11 years 30 to 82
12 to 17 years 26 to 44
18 years and above 22 to 43

MONOCYTES
0 to 1 day 2 to 10
2 to 7 days 2 to 12
8 to 29 days 3 to 12
1 to 5 months 3 to 10
6 to 11 months 0 to 7
1 to 5 years 0 to 6
6 to 11 years 0 to 5
12 to 17 years 0 to 5
18 years and above 0 to 7

EOSINOPHIL
0 to 1 day 0 to 3
2 to 7 days 0 to 5
8 to 29 days 0 to 5
1 to 5 months 1 to 5
6 to 11 months 1 to 4
1 to 5 years 0 to 4
6 to 11 years 0 to 4
12 to 17 years 0 to 4
18 years and above 0 to 4

BASOPHIL
0 to 1 day 0 to 2
2 to 7 days 0 to 1
8 to 29 days 0 to 1
1 to 5 months 0 to 1
6 to 11 months 0 to 1
1 to 5 years 0 to 1
6 to 11 years 0 to 1
12 to 17 years 0 to 1
18 years and above 0 to 1

Hemoglobin: g/dL
Hematocrit: %
RBC: x106/uL
WBC: x103/uL
MCH: pg
MCHC: %
MCV: um3
Neutrophil: %
Stab/Band: %
Lymphocyte: %
Monocyte: %
Eosinophil: %
Basophil: %

Complete Blood Count

A complete blood count (CBC) is performed on automated hematology profiling instruments and includes the RBC, WBC, and platelet measurements. It is a blood test used to evaluate the overall health and detect a wide range of disorders, including anemia, infection and leukemia.

Source: RODAK’s Hematology Clinical Principles and Applications 5th Edition

TEST DETAILS
MLLI CODE	JERCBC

Assay Timetable
Test Category	Test Schedule	Results Availability
STAT	Daily	Within 20 minutes

Assay Information
Methodology	RBC, Hct, and Platelet Count - Impedance Method with hydrodynamic focusing •Hemoglobin - non-cyanide determination •WBC and differential count - fluorescence flow cytometry (hydrodynamically focused)
Synonyms	Not Applicable
Acronyms	CBC- Complete Blood Count

SPECIMEN PREPARATION
Specimen Type	Specimen Required Volume	Specimen Container	Specimen Storage and Stability	Patient Preparation
Whole blood	2 mL	5	Storage: 2 to 8˚C Stability: 24 hours	No patient preparation
NOTE	•Offered to MMC ONLY.

Conventional Reference Range

Conventional Unit

HEMOGLOBIN
0 to 1 day 135 to 225
2 to 7 days 135 to 225
8 to 29 days 100 to 215
1 to 5 months 100 to 180
6 to 11 months 95 to 135
1 to 5 years 105 to 135
6 to 11 years 115 to 135
12 to 17 years 115 to 135
18 years and above Female 123 to 153
18 years and above Male 140 to 165