Biochemistry tests in Dubai & UAE

Compare available Biochemistry tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

Tests in this category

1,113

Listed price range

450.00–30,000.00 AED

Clinical preparation

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Biochemistry test prices

Showing 61–75 of 1,113 matching tests.

Biochemistry diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-132 Alcohol Ethyl Glucuronide (EtG) & Ethyl Sulphate (EtS) Urine Test This test measures the primary metabolites of ethanol (alcohol) in urine, providing a direct indication of alcohol consumption.	Urine (random clean catch)	Sample Friday by 6 PM; report Saturday (same-weekend results)	600.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Ethyl Glucuronide (EtG)", "Ethyl Sulphate (EtS)"] Parameters [{"name": "Ethyl Glucuronide (EtG)", "reference_range": null}, {"name": "Ethyl Sulphate (EtS)", "reference_range": null}] Preparation ["Avoid alcohol-containing mouthwash, hand sanitizers, or herbal tonics for 24 hours before specimen collection."] Indications ["Compliance monitoring", "Addiction medicine", "Legal verification of abstinence", "Employment screening"] Measurement technique Confirm with laboratory Codes LOINC: 58355-3 ICD-10: F10.10, F10.20, Z02.83 Clinical summary This test measures the primary metabolites of ethanol (alcohol) in urine, providing a direct indication of alcohol consumption.
TEST-5950 ALDH2 Gene Acute Alcohol Sensitivity Genetic Test This genetic test evaluates functional variants within the ALDH2 gene to determine an individual's capacity to metabolize acetaldehyde, the toxic intermediate of alcohol.	Peripheral Whole Blood	21–28 Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Functional variants in the ALDH2 gene", "Acetaldehyde metabolism capacity"] Parameters [] Preparation [] Indications ["Assessment of acute alcohol sensitivity", "Risk assessment for alcohol-related health issues", "Personalized advice on alcohol intake"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Z13.89 Clinical summary This genetic test evaluates functional variants within the ALDH2 gene to determine an individual's capacity to metabolize acetaldehyde, the toxic intermediate of alcohol.
TEST-6198 ALDH4A1 Gene Hyperprolinemia Type 2 Genetic Test This genetic test identifies pathogenic variants in the ALDH4A1 gene associated with Hyperprolinemia type 2.	Whole Blood (peripheral)	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the ALDH4A1 gene"] Parameters [] Preparation ["No fasting required", "Pre-test genetic counselling session mandatory"] Indications ["Suspected Hyperprolinemia type 2", "Family history of Hyperprolinemia type 2", "Evaluation of inborn errors of metabolism"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: E72.52 Clinical summary This genetic test identifies pathogenic variants in the ALDH4A1 gene associated with Hyperprolinemia type 2.
TEST-6049 ALDH6A1 Gene Methylmalonate Semialdehyde Dehydrogenase Deficiency Genetic Test This genetic test identifies pathogenic variants in the ALDH6A1 gene associated with methylmalonate semialdehyde dehydrogenase deficiency.	Whole Blood	3–4 weeks with interim reports	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the ALDH6A1 gene", "Enzyme deficiency related to ALDH6A1"] Parameters [] Preparation ["No fasting required", "Provide detailed clinical history", "Provide a three-generation pedigree chart"] Indications ["Suspected methylmalonate semialdehyde dehydrogenase deficiency", "Family history of the disorder", "Ambiguous biochemical results", "Carrier screening"] Measurement technique Confirm with laboratory Codes LOINC: 94046-3 ICD-10: E70.8 Clinical summary This genetic test identifies pathogenic variants in the ALDH6A1 gene associated with methylmalonate semialdehyde dehydrogenase deficiency.
TEST-147 Aldosterone/Renin Direct Ratio (Plasma) Test This diagnostic test evaluates the ratio of aldosterone to direct renin in plasma to screen for primary aldosteronism.	Plasma (EDTA)	Same-day report (Tuesday and Friday by 11:00 AM)	1,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Aldosterone concentration (ng/dL)", "Direct Renin concentration (μg/L)", "Aldosterone/Renin Ratio"] Parameters [{"name": "Aldosterone", "reference_range": "ng/dL (Specific range varies by lab, typically 1-30)"}, {"name": "Direct Renin", "reference_range": "μg/L (Specific range varies by lab, typically 1-10)"}, {"name": "Aldosterone/Renin Ratio", "reference_range": "Ratio (Specific range varies by lab, typically 10-30)"}] Preparation ["Maintain upright posture (standing or walking) for at least 2 hours before sample collection.", "Follow physician's instructions regarding temporary medication adjustments.", "Avoid high-sodium meals for 24 hours prior.", "Inform the phlebotomist of all current prescriptions."] Indications ["Screening for primary aldosteronism in patients with hypertension", "Evaluation of resistant hypertension", "Investigation of unexplained hypokalemia"] Measurement technique Confirm with laboratory Codes LOINC: 45336-9 ICD-10: E26.0 Clinical summary This diagnostic test evaluates the ratio of aldosterone to direct renin in plasma to screen for primary aldosteronism.
TEST-6365 ALG12 Gene Glycosylation Disorder Type 1G Genetic Test This genetic test screens the entire ALG12 gene for pathogenic variants associated with Congenital Disorder of Glycosylation Type 1G (ALG12-CDG). It uses Next-Generation Sequencing...	Whole Blood (EDTA) – Peripheral Venous Blood	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the ALG12 gene", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy number variants (CNVs)"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed therapy"] Indications ["Suspected Congenital Disorder of Glycosylation Type 1G (ALG12-CDG)", "Individuals with clinical features suggestive of ALG12-CDG", "Family history of ALG12-CDG"] Measurement technique Confirm with laboratory Codes LOINC: 92789-1 ICD-10: E77.8 Clinical summary This genetic test screens the entire ALG12 gene for pathogenic variants associated with Congenital Disorder of Glycosylation Type 1G (ALG12-CDG). It uses Next-Generation Sequencing (NGS) with confirmatory Sanger sequencing.
TEST-4462 ALG6 Gene Glycosylation Disorder Type 1C Genetic Test This genetic test evaluates the ALG6 gene for mutations associated with Congenital Disorder of Glycosylation Type 1c.	Peripheral whole blood (EDTA) or FTA card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Mutations in the ALG6 gene", "Single-nucleotide variants", "Insertions", "Deletions", "Splice-site alterations"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any current medications"] Indications ["Suspected Congenital Disorder of Glycosylation Type 1c", "Family history of CDG-1c", "Neurological symptoms consistent with CDG-1c"] Measurement technique Confirm with laboratory Codes LOINC: 82939-0 ICD-10: E77.8 Clinical summary This genetic test evaluates the ALG6 gene for mutations associated with Congenital Disorder of Glycosylation Type 1c.
TEST-6301 ALG9 Gene Genetic Test for Congenital Disorder of Glycosylation Type 1L (CDG-IL) This genetic test identifies mutations in the ALG9 gene associated with Congenital Disorder of Glycosylation Type 1L (CDG-IL).	Whole blood (EDTA), extracted DNA, or FTA card	15–20 working days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ALG9 gene sequence", "Copy number variations in ALG9 gene"] Parameters [] Preparation ["Genetic counselling with pedigree chart mandatory prior to testing", "No fasting required for blood draw"] Indications ["Suspected Congenital Disorder of Glycosylation Type 1L (CDG-IL)", "Family history of CDG-IL"] Measurement technique Confirm with laboratory Codes LOINC: 81265-0 ICD-10: E77.8 Clinical summary This genetic test identifies mutations in the ALG9 gene associated with Congenital Disorder of Glycosylation Type 1L (CDG-IL).
TEST-139 Alkaline Phosphatase (ALP) Isoenzymes Test This diagnostic test evaluates the different tissue sources of alkaline phosphatase enzyme activity in the blood.	Serum	Next business day (sample received by Thursday 9 AM)	1,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Liver ALP fraction", "Bone ALP fraction", "Intestinal ALP fraction", "Placental ALP fraction"] Parameters [{"name": "Liver ALP", "reference_range": null}, {"name": "Bone ALP", "reference_range": null}, {"name": "Intestinal ALP", "reference_range": null}, {"name": "Placental ALP", "reference_range": null}] Preparation ["Overnight fasting required (10–12 hours)", "Do not discontinue prescribed medication without consulting your physician"] Indications ["Investigation of elevated total ALP", "Suspected liver disease", "Suspected bone disease", "Monitoring response to treatment for liver or bone conditions"] Measurement technique Confirm with laboratory Codes LOINC: 2276-1 ICD-10: R74.8 Clinical summary This diagnostic test evaluates the different tissue sources of alkaline phosphatase enzyme activity in the blood.
TEST-1 Alkaline Phosphatase, Bone-Specific (BSAP) Test This diagnostic test evaluates the level of bone-specific alkaline phosphatase in the serum, indicating osteoblast activity and bone formation.	Serum	10 days	900.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Bone-specific alkaline phosphatase (BSAP)", "Osteoblast activity", "Bone formation rate"] Parameters [{"name": "Alkaline Phosphatase, Bone-Specific", "reference_range": null}] Preparation ["No special preparation or fasting is required", "Inform phlebotomist about current medications and supplements"] Indications ["Diagnosis and monitoring of osteoporosis", "Diagnosis and monitoring of Paget's disease", "Detection and monitoring of bone metastases", "Evaluation of fracture healing"] Measurement technique Confirm with laboratory Codes LOINC: 17876-7 ICD-10: M81.0 Clinical summary This diagnostic test evaluates the level of bone-specific alkaline phosphatase in the serum, indicating osteoblast activity and bone formation.
TEST-154 Alkaptonuria Urine Quantitative Test This test quantitatively measures the level of homogentisic acid (HGA) in a urine sample.	Random Urine	5 working days (sample daily by 5 pm)	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Homogentisic acid (HGA) levels", "Homogentisate 1,2-dioxygenase deficiency"] Parameters [{"name": "Homogentisic acid (HGA)", "reference_range": null}] Preparation ["No special preparation required", "Collect 15 mL random urine in a sterile screw-capped container without preservative", "Keep refrigerated or frozen during transport"] Indications ["Diagnosis of alkaptonuria", "Monitoring of alkaptonuria treatment response"] Measurement technique Confirm with laboratory Codes LOINC: 5813-5 ICD-10: E70.2 Clinical summary This test quantitatively measures the level of homogentisic acid (HGA) in a urine sample.
TEST-4974 ALOXE3 Gene Test This diagnostic test evaluates the ALOXE3 gene for mutations associated with nonbullous congenital ichthyosiform erythroderma.	Peripheral Whole Blood	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Point mutations in ALOXE3 gene", "Small indels in ALOXE3 gene", "Copy number variants in ALOXE3 gene"] Parameters [] Preparation [] Indications ["Diagnosis of nonbullous congenital ichthyosiform erythroderma", "Genetic counseling for families with a history of the condition"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Q80.2 Clinical summary This diagnostic test evaluates the ALOXE3 gene for mutations associated with nonbullous congenital ichthyosiform erythroderma.
TEST-159 Alpha-1-Acid Glycoprotein (AGP) Test This diagnostic test evaluates the concentration of Alpha-1-Acid Glycoprotein (AGP) in the serum.	Serum	2–3 Weeks	1,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Alpha-1-Acid Glycoprotein (AGP) levels", "Acute phase response", "Inflammation markers", "Tumor activity"] Parameters [{"name": "Alpha-1-Acid Glycoprotein (AGP)", "reference_range": null}] Preparation ["Overnight fasting required", "Collect sample in a 2 mL plain Red Top tube (no SST gel)", "Duly filled Test Send Out Consent Form (Form 35) is mandatory"] Indications ["Monitoring inflammation", "Tumor monitoring", "Drug binding assessment", "Nutritional status evaluation"] Measurement technique Confirm with laboratory Codes LOINC: 1917-6 ICD-10: R79.89 Clinical summary This diagnostic test evaluates the concentration of Alpha-1-Acid Glycoprotein (AGP) in the serum.
TEST-163 Alpha-1-Antitrypsin (AAT) Phenotype Test This test evaluates the specific protein variants (Pi types) of Alpha-1-Antitrypsin in the blood.	Serum	2–3 weeks after sample receipt by the 7th of the month	2,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Alpha-1-Antitrypsin protein variants (Pi types)", "Quantitative and qualitative protein variants"] Parameters [{"name": "Alpha-1-Antitrypsin Phenotype", "reference_range": null}] Preparation ["No fasting required", "Complete Test Send Out Consent Form (Form 35)"] Indications ["Diagnosis of alpha-1 antitrypsin deficiency", "Assessment of risk for lung and liver disease", "Evaluation of unexplained respiratory or liver conditions"] Measurement technique Confirm with laboratory Codes LOINC: 55014-4 ICD-10: E88.01 Clinical summary This test evaluates the specific protein variants (Pi types) of Alpha-1-Antitrypsin in the blood.
TEST-156 Alpha-1-Antitrypsin Quantitation (AAT) Test This diagnostic test evaluates the quantity of Alpha-1-Antitrypsin protein in the serum.	Serum	Same day (Mon/Thu by 4 pm)	550.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Alpha-1-Antitrypsin protein levels", "Genetic predisposition to AAT deficiency"] Parameters [{"name": "Alpha-1-Antitrypsin", "reference_range": "null"}] Preparation ["Fast from food for two hours before sample collection", "Inform the phlebotomist about all current medications"] Indications ["Screening for genetic AAT deficiency", "Evaluation of unexplained liver disease", "Investigation of early-onset emphysema", "Family history of AAT deficiency"] Measurement technique Confirm with laboratory Codes LOINC: 33914-0 ICD-10: E88.01 Clinical summary This diagnostic test evaluates the quantity of Alpha-1-Antitrypsin protein in the serum.

Category overview

Biochemistry: overview

Seeking clarity about your body's essential functions is vital for long-term well-being. At DNA Labs UAE, our Biochemistry services utilize advanced automated analyzers to evaluate enzymes, proteins, and metabolites in your blood. Whether you need routine metabolic panels or specialized biochemical testing in the UAE, these tests provide critical data to guide your physician's medical plan. As a leading diagnostic lab in Dubai and the UAE, we guarantee strict confidentiality and rapid, accurate turnaround times. Take charge of your health today. Explore our biochemistry diagnostics below, schedule a convenient home sample collection, or contact our specialists to book your test.

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Biochemistry tests in Dubai & UAE

Biochemistry test prices

Biochemistry: overview

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