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.

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1,113

Listed price range

450.00–30,000.00 AED

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Biochemistry test prices

Showing 106–120 of 1,113 matching tests.

Biochemistry diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5987 APOA1 Gene Amyloidosis, Familial Visceral Genetic Test This genetic test screens for pathogenic variants in the APOA1 gene associated with familial visceral amyloidosis.	Whole Blood (EDTA) or FTA Card	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 APOA1 gene", "Single nucleotide variants", "Small insertions/deletions", "Copy number changes"] Parameters [] Preparation ["No specific fasting required.", "Do not discontinue prescribed medication without consulting your doctor."] Indications ["Confirmation of suspected familial visceral amyloidosis", "Genetic risk assessment for family members of affected individuals", "Evaluation of unexplained organ dysfunction potentially related to amyloid deposition"] Measurement technique Confirm with laboratory Codes LOINC: 21647-2 ICD-10: E85.0 Clinical summary This genetic test screens for pathogenic variants in the APOA1 gene associated with familial visceral amyloidosis.
TEST-6197 APOB Gene Hypercholesterolaemia Type B (Autosomal Dominant) Genetic Test This genetic test identifies pathogenic variants in the APOB gene associated with autosomal dominant familial hypercholesterolaemia type B.	Whole blood (EDTA), extracted DNA, or dried blood spot on FTA card	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 APOB gene", "Genetic predisposition to hypercholesterolaemia type B"] Parameters [] Preparation ["No specific fasting required", "No medication adjustments needed unless advised by physician"] Indications ["Diagnosis of autosomal dominant familial hypercholesterolaemia type B", "Cardiovascular risk stratification", "Cascade testing for family members"] Measurement technique Confirm with laboratory Codes LOINC: 94046-6 ICD-10: E78.01 Clinical summary This genetic test identifies pathogenic variants in the APOB gene associated with autosomal dominant familial hypercholesterolaemia type B.
TEST-328 APOE Genotyping Test This test evaluates genetic variations in the apolipoprotein E gene (APOE) associated with Alzheimer's disease and cardiovascular risk.	Whole blood (EDTA tube, 4 mL)	10 Working Days	4,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["APOE gene variations (ε2, ε3, ε4 alleles)"] Parameters [] Preparation [] Indications ["Risk assessment for late-onset Alzheimer's disease", "Assessment of genetic predisposition to cardiovascular conditions"] Measurement technique Confirm with laboratory Codes LOINC: 21637-2 ICD-10: Z13.858 Clinical summary This test evaluates genetic variations in the apolipoprotein E gene (APOE) associated with Alzheimer's disease and cardiovascular risk.
TEST-3005 AR Gene Hypospadias Type 1, X-Linked Genetic Test This diagnostic test evaluates the androgen receptor (AR) gene for pathogenic variants associated with X-linked hypospadias type 1.	Whole Blood (Lavender Top EDTA Tube) or Dried Blood Spot (FTA Card)	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 AR gene", "Single nucleotide variants (SNVs)", "Small insertions and deletions (indels)", "Copy number variations (CNVs)"] Parameters [] Preparation ["No specific fasting required", "Avoid recent blood transfusions"] Indications ["Diagnosis of X-linked hypospadias type 1", "Genetic counseling for families with affected individuals", "Prenatal diagnosis in high-risk pregnancies"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q54.0 Clinical summary This diagnostic test evaluates the androgen receptor (AR) gene for pathogenic variants associated with X-linked hypospadias type 1.
TEST-6008 ARG1 Gene Arginase Deficiency Genetic Test This genetic test identifies pathogenic variants in the ARG1 gene associated with arginase deficiency.	Peripheral whole blood (EDTA or FTA card)	3–4 weeks from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the ARG1 gene", "Coverage of coding exons, splice sites, and deep intronic regions"] Parameters [] Preparation ["No specific fasting required", "Inform lab of recent blood transfusions"] Indications ["Suspected arginase deficiency", "Family history of urea cycle disorders", "Neurological symptoms in infants or children"] Measurement technique Confirm with laboratory Codes LOINC: 76527-5 ICD-10: E72.21 Clinical summary This genetic test identifies pathogenic variants in the ARG1 gene associated with arginase deficiency.
TEST-330 Arginase Test This test measures the functional activity of the arginase enzyme within red blood cells to diagnose arginase deficiency.	Whole blood (EDTA tube)	3 business days	600.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Arginase enzyme activity", "Urea cycle function"] Parameters [{"name": "Arginase Activity", "reference_range": null}] Preparation ["No specific fasting required", "Inform lab if patient is on arginine supplementation or dialysis"] Indications ["Suspected arginase deficiency (ARG1)", "Evaluation of urea cycle disorders", "Inconclusive plasma amino acid results"] Measurement technique Confirm with laboratory Codes LOINC: 18428-3 ICD-10: E72.21 Clinical summary This test measures the functional activity of the arginase enzyme within red blood cells to diagnose arginase deficiency.
TEST-3903 ARL6 Gene Bardet‑Biedl Syndrome Type 3 Genetic Test This test analyzes the ARL6 gene for pathogenic variants associated with Bardet‑Biedl Syndrome Type 3.	Whole blood (2‑5 mL in EDTA tube), extracted DNA (≥1 µg), or one drop of blood on FTA card	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 ARL6 gene"] Parameters [] Preparation ["A detailed clinical history and a genetic counseling session to draw a pedigree chart of affected family members are required before sample collection."] Indications ["Diagnostic confirmation of Bardet‑Biedl Syndrome Type 3", "Family screening for ARL6 variants"] Measurement technique Confirm with laboratory Codes LOINC: 51990-0 ICD-10: Q87.8 Clinical summary This test analyzes the ARL6 gene for pathogenic variants associated with Bardet‑Biedl Syndrome Type 3.
TEST-335 ARSENIC 24 HOUR URINE Test This test measures the total amount of arsenic excreted in urine over a 24-hour period to assess chronic exposure.	24-Hour Urine	Next day (sample received by 6 PM)	550.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Total arsenic excretion", "Chronic arsenic exposure"] Parameters [{"name": "Total Arsenic", "reference_range": "0.1 µg/L"}] Preparation ["Avoid seafood and herbal supplements for 3 days prior", "Do not discontinue prescribed medication without consulting your doctor", "Use only powderless gloves during collection"] Indications ["Monitoring industrial workers", "Evaluating unexplained neuropathies", "Confirming environmental heavy metal burden"] Measurement technique Confirm with laboratory Codes LOINC: 21090-5 ICD-10: T56.1 Clinical summary This test measures the total amount of arsenic excreted in urine over a 24-hour period to assess chronic exposure.
TEST-336 Arsenic Blood Test This diagnostic test evaluates the concentration of total arsenic in a whole blood sample.	Whole blood (peripheral vein)	1 business day (next-day by 6 PM)	550.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Total arsenic concentration", "Trace element levels"] Parameters [{"name": "Total Arsenic", "reference_range": "0.1 µg/L"}] Preparation ["Avoid seafood, herbal supplements, and arsenic-containing medications for 3 days prior to collection.", "No fasting required; hydrate normally.", "Wear short sleeves for easy venous access."] Indications ["Suspected acute or chronic arsenic poisoning", "Monitoring occupational exposure", "Monitoring environmental exposure", "Proactive health assessment"] Measurement technique Confirm with laboratory Codes LOINC: 1346-2 ICD-10: T57.0X1A, Z13.83 Clinical summary This diagnostic test evaluates the concentration of total arsenic in a whole blood sample.
TEST-338 Arsenic Random Urine Test This test quantifies total arsenic metabolites in urine to assess recent exposure.	Random Urine	Next-day report (sample by 6 pm)	550.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Total inorganic arsenic metabolites", "Total organic arsenic metabolites"] Parameters [{"name": "Total Arsenic", "reference_range": "0.1 µg/L LOD"}] Preparation ["Abstain from all seafood and herbal supplements strictly for 3 days prior.", "If you received MRI contrast or iodine dye, wait 96 hours before collecting the sample.", "Use only the provided metal-free, acid-washed container."] Indications ["Occupational health surveillance", "Chelation therapy monitoring", "Assessing detoxification protocol efficacy", "Suspected acute inorganic arsenic poisoning"] Measurement technique Confirm with laboratory Codes LOINC: 5587-8 ICD-10: Z77.010, T57.0X1A Clinical summary This test quantifies total arsenic metabolites in urine to assess recent exposure.
TEST-5027 ARX Gene Mental Retardation, X‑Linked Type 29 Genetic Test This test evaluates the ARX gene for pathogenic variants associated with X-linked intellectual disability type 29 and related neurological conditions.	Peripheral Whole Blood (1–2 mL EDTA), Extracted DNA, or Dried Blood Spot (FTA Card)	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 ARX gene", "Point mutations", "Small insertions/deletions (indels)", "Splice variants"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist if child cannot tolerate venipuncture for FTA card collection"] Indications ["Diagnosis of X-linked intellectual disability type 29", "Carrier testing in females with family history", "Evaluation of developmental delay, seizures, or movement disorders"] Measurement technique Confirm with laboratory Codes LOINC: 94221-1 ICD-10: F78.9 Clinical summary This test evaluates the ARX gene for pathogenic variants associated with X-linked intellectual disability type 29 and related neurological conditions.
TEST-6294 ASAH1 Gene Sequencing for Farber Disease (Genetic Test) This test sequences the ASAH1 gene to detect pathogenic variants associated with Farber lipogranulomatosis.	Whole blood (EDTA tube), extracted DNA, or FTA card	3–4 weeks (with genetic counselling)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the ASAH1 gene", "Copy Number Variations (CNV) in ASAH1"] Parameters [] Preparation ["No specific fasting required", "Genetic counselling session required before testing"] Indications ["Suspicion of Farber lipogranulomatosis", "Family history of Farber disease", "Need for definitive molecular diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 81201-4 ICD-10: E75.22 Clinical summary This test sequences the ASAH1 gene to detect pathogenic variants associated with Farber lipogranulomatosis.
TEST-3669 ASB10 Gene Glaucoma, Open-Angle Type 1F Genetic Test This genetic test evaluates the ASB10 gene for pathogenic variants associated with primary open-angle glaucoma (POAG). It identifies individuals at increased lifetime risk for deve...	Peripheral Whole 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 ASB10 gene", "Genetic predisposition to Primary Open-Angle Glaucoma (POAG)"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication without consulting your doctor"] Indications ["Individuals with a first-degree relative diagnosed with POAG", "Risk stratification for POAG", "Personalized management planning"] Measurement technique Confirm with laboratory Codes LOINC: 104198-4 ICD-10: H40.11, Z13.5 Clinical summary This genetic test evaluates the ASB10 gene for pathogenic variants associated with primary open-angle glaucoma (POAG). It identifies individuals at increased lifetime risk for developing this condition.
TEST-6013 ASL Gene (Argininosuccinic Aciduria) Genetic Test This genetic test identifies pathogenic variants within the ASL gene, confirming or ruling out a diagnosis of Argininosuccinic Aciduria.	Whole Blood (EDTA), Extracted DNA, or FTA Card Dried Blood Spot	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 ASL gene", "Single nucleotide variants (SNVs)", "Small insertions and deletions (indels)", "Splice-site mutations"] Parameters [] Preparation ["Pre-test genetic counseling is mandatory", "Detailed pedigree chart of family medical history must be reviewed", "Testing of minors requires informed parental/guardian consent"] Indications ["Clinical symptoms suggestive of Argininosuccinic Aciduria", "Family history of the disease", "Carrier screening", "Pre-conception risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 90237-0 ICD-10: E72.53 Clinical summary This genetic test identifies pathogenic variants within the ASL gene, confirming or ruling out a diagnosis of Argininosuccinic Aciduria.
TEST-6017 ASNS Gene Asparagine Synthetase Deficiency Genetic Test This genetic test identifies pathogenic variants in the ASNS gene, confirming asparagine synthetase deficiency.	Whole Blood (Peripheral)	3–4 Weeks (expedited possible)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the ASNS gene", "SNVs, indels, and CNVs"] Parameters [] Preparation ["No fasting is required.", "A mandatory pre-genetic counselling session is conducted."] Indications ["Clinical suspicion of asparagine synthetase deficiency", "Patients with microcephaly, refractory epilepsy, and developmental delay"] Measurement technique Confirm with laboratory Codes LOINC: 94495-4 ICD-10: E79.8 Clinical summary This genetic test identifies pathogenic variants in the ASNS gene, confirming asparagine synthetase deficiency.

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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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