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

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Biochemistry test prices

Showing 886–900 of 1,113 matching tests.

Biochemistry diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4351 SDHA Gene Dilated Cardiomyopathy Type 1GG Genetic Test This test evaluates the SDHA gene for pathogenic variants associated with Dilated Cardiomyopathy Type 1GG.	Whole Blood (Peripheral) – Standard Venipuncture or 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 SDHA gene", "Likely pathogenic variants in the SDHA gene", "Copy Number Variations (CNVs) in the SDHA gene"] Parameters [{"name": "SDHA Gene Analysis", "reference_range": "Negative for pathogenic/likely pathogenic variants"}] Preparation ["No fasting or special diet required", "Mandatory pre-test genetic counselling session required"] Indications ["Definitive diagnosis of Dilated Cardiomyopathy Type 1GG", "Family cascade screening for SDHA variants", "Guiding prophylactic clinical interventions", "Evaluation of patients with unexplained cardiomyopathy"] Measurement technique Confirm with laboratory Codes LOINC: 94800-2 ICD-10: I42.8 Clinical summary This test evaluates the SDHA gene for pathogenic variants associated with Dilated Cardiomyopathy Type 1GG.
TEST-4646 SDHA Gene Leigh Syndrome Genetic Test This test evaluates the SDHA gene for mutations associated with Leigh syndrome, a severe mitochondrial disorder.	Blood, Extracted DNA, 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 ["SDHA gene sequence", "Copy Number Variations (CNVs) in SDHA gene"] Parameters [] Preparation ["No specific fasting required.", "No medication or diet restrictions."] Indications ["Clinical suspicion of Leigh syndrome", "Family history of mitochondrial disorders", "Need for accurate diagnosis to guide therapy", "Family risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 95219-5 ICD-10: G31.81 Clinical summary This test evaluates the SDHA gene for mutations associated with Leigh syndrome, a severe mitochondrial disorder.
TEST-2110 SDHD Gene Carcinoid Tumor (Intestinal) Genetic Test This genetic test analyzes the SDHD gene for mutations associated with an increased risk of hereditary intestinal carcinoid tumors and paragangliomas.	Peripheral whole blood, buccal swab, or FTA card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SDHD gene mutations", "Germline variants"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Individuals with a personal or family history of intestinal carcinoid tumors or paragangliomas", "Screening for hereditary predisposition"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: C7A.0, C7A.1, C7A.2 Clinical summary This genetic test analyzes the SDHD gene for mutations associated with an increased risk of hereditary intestinal carcinoid tumors and paragangliomas.
TEST-1950 SDHD Gene Paraganglioma Type 1 Genetic Test This test evaluates the SDHD gene for germline mutations associated with hereditary paraganglioma type 1 syndrome.	Peripheral Whole Blood	3 – 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SDHD gene sequence", "Germline mutations"] Parameters [] Preparation ["Genetic counseling session required", "No fasting or special diet required"] Indications ["Personal or family history of paragangliomas", "Personal or family history of pheochromocytomas", "Early-onset sensorineural deafness", "Known familial SDHD mutation"] Measurement technique Confirm with laboratory Codes LOINC: 94483-2 ICD-10: D44.7 Clinical summary This test evaluates the SDHD gene for germline mutations associated with hereditary paraganglioma type 1 syndrome.
TEST-3498 SECISBP2 Gene Thyroid Hormone Metabolism Abnormalities Genetic Test This genetic test detects pathogenic variants in the SECISBP2 gene associated with thyroid hormone metabolism abnormalities.	Whole Blood (EDTA)	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 SECISBP2 gene", "Thyroid hormone metabolism disruption", "Selenoprotein synthesis disruption"] Parameters [] Preparation ["No specific fasting required", "Avoid sample collection during acute illness"] Indications ["Suspected genetic cause of thyroid hormone metabolism abnormalities", "Family history of related disorders", "Guiding targeted therapy", "Family cascade screening"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: E07.89 Clinical summary This genetic test detects pathogenic variants in the SECISBP2 gene associated with thyroid hormone metabolism abnormalities.
TEST-1305 Secretin Stimulation Test for Gastrin (Gastrinoma Diagnosis) This diagnostic test evaluates the body's response to secretin stimulation by measuring serial serum gastrin levels to identify gastrinoma.	Serum (peripheral whole blood)	Same day (if collected before 11 AM Monday/Thursday)	1,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Serum Gastrin Levels", "Response to Secretin Provocation"] Parameters [{"name": "Basal Gastrin", "reference_range": null}, {"name": "Gastrin at 5 min post-secretin", "reference_range": null}, {"name": "Gastrin at 10 min post-secretin", "reference_range": null}, {"name": "Gastrin at 15 min post-secretin", "reference_range": null}, {"name": "Gastrin at 20 min post-secretin", "reference_range": null}, {"name": "Gastrin at 25 min post-secretin", "reference_range": null}, {"name": "Gastrin at 30 min post-secretin", "reference_range": null}] Preparation ["Fast overnight (minimum 8 hours, water allowed)", "Remain comfortably at rest throughout the procedure", "Do not discontinue prescribed medications without consulting your physician"] Indications ["Suspected gastrinoma (Zollinger-Ellison syndrome)", "Evaluation of unexplained hypergastrinemia", "Differentiation of gastrinoma from pseudo-hypergastrinemia"] Measurement technique Confirm with laboratory Codes LOINC: 35453-8 ICD-10: E16.4 Clinical summary This diagnostic test evaluates the body's response to secretin stimulation by measuring serial serum gastrin levels to identify gastrinoma.
TEST-3099 Selenium 24-Hour Urine Test This test measures the total amount of selenium excreted in urine over 24 hours to assess whole-body selenium status and metabolic balance.	24-Hour Urine	Next Day (if sample is received by 6 PM)	800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Total selenium excretion (µg/24h)", "Whole-body selenium status", "Metabolic turnover of selenium"] Parameters [{"name": "Selenium (Total, 24-Hour Urine)", "reference_range": "DHA-established reference ranges calibrated for the UAE population"}] Preparation ["Avoid iodine-based and gadolinium contrast agents for at least 96 hours prior to collection.", "Discard the first morning void on the collection day.", "Collect all subsequent urine for exactly 24 hours, including the first void of the following morning.", "Keep the container refrigerated throughout the collection period.", "Record the total volume on the provided requisition form.", "Wear the included powderless gloves during collection."] Indications ["Diagnosing nutritional selenium deficiency", "Evaluating chronic industrial toxic exposure", "Monitoring patients with complex gastrointestinal or renal disorders", "Assessing unexplained neuro-metabolic presentations"] Measurement technique Confirm with laboratory Codes LOINC: 56822-1 ICD-10: E59, Z13.22 Clinical summary This test measures the total amount of selenium excreted in urine over 24 hours to assess whole-body selenium status and metabolic balance.
TEST-3102 Selenium Serum Test This diagnostic test evaluates the concentration of selenium, an essential trace mineral, in the patient's serum.	Serum	Next day by 6 PM	850.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Selenium levels in serum", "Trace element status"] Parameters [{"name": "Selenium", "reference_range": "0.1 µg/L"}] Preparation ["No fasting required.", "Avoid contrast media (Gadolinium, Iodine, Barium) for 96 hours prior.", "Refrain from selenium-containing supplements for 24 hours prior unless directed by a doctor.", "Ensure metal-free collection supplies are used."] Indications ["Suspected selenium deficiency", "Suspected selenium toxicity", "Monitoring nutritional status", "Evaluating exposure to industrial toxins", "Investigating unexplained symptoms potentially linked to selenium imbalance"] Measurement technique Confirm with laboratory Codes LOINC: 5685-4 ICD-10: E59, Z13.8 Clinical summary This diagnostic test evaluates the concentration of selenium, an essential trace mineral, in the patient's serum.
TEST-3120 Selenium, Random Urine Test This test evaluates the concentration of selenium excreted in urine, reflecting recent exposure and nutritional status.	Random Urine	Next day by 6 PM	850.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Selenium excretion", "Recent selenium exposure"] Parameters [{"name": "Selenium", "reference_range": "0.1 µg/L (LOD)"}] Preparation ["Use only the metal-free kit provided", "Avoid Gadolinium, Iodine, or Barium contrast media for 96 hours prior", "Wear powderless gloves during collection"] Indications ["Occupational exposure surveillance", "Nutritional assessment", "Monitoring potential selenium toxicity", "Evaluating selenium deficiency"] Measurement technique Confirm with laboratory Codes LOINC: 5700-3 ICD-10: Z77.098, T56.8X1A, Z10.0 Clinical summary This test evaluates the concentration of selenium excreted in urine, reflecting recent exposure and nutritional status.
TEST-3670 SEMA3A Gene (Kallmann Syndrome) Sequencing Test This test evaluates the SEMA3A gene for mutations associated with Kallmann syndrome.	Peripheral Whole Blood	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SEMA3A gene variants", "Pathogenic mutations"] Parameters [] Preparation [] Indications ["Diagnosis of Kallmann syndrome", "Genetic counseling for Kallmann syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: E23.0 Clinical summary This test evaluates the SEMA3A gene for mutations associated with Kallmann syndrome.
TEST-3104 Serotonin (5-Hydroxytryptamine), 24-Hour Urine Test This diagnostic test evaluates the total excretion of serotonin (5-Hydroxytryptamine) in urine over a 24-hour period.	24-Hour Urine	2 working days after sample receipt	900.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Total urinary serotonin excretion", "Neuroendocrine activity"] Parameters [{"name": "Serotonin (5-HT)", "reference_range": null}] Preparation ["Avoid bananas, walnuts, tomatoes, pineapples, plums, gooseberries, mirabelles, melons, avocados, aubergines, kiwi fruits for 48 hours before collection.", "Avoid Methocarbamol, mephenesin, guaifenesin, paracetamol, salicylic acid (aspirin) before collection; consult physician for alternatives.", "Avoid strenuous exercise 48 hours before and during collection.", "Use lab-provided container with 50% HCl.", "Record total 24-hour volume on the request form.", "Keep specimen refrigerated or frozen."] Indications ["Diagnosis of carcinoid syndrome", "Diagnosis of neuroendocrine tumours"] Measurement technique Confirm with laboratory Codes LOINC: 32387-2 ICD-10: E34.0 Clinical summary This diagnostic test evaluates the total excretion of serotonin (5-Hydroxytryptamine) in urine over a 24-hour period.
TEST-3127 Serotonin (5‑HT) Random Urine Test This diagnostic test evaluates the level of serotonin (5-hydroxytryptamine) in a random urine sample to help diagnose neuroendocrine tumours and carcinoid syndrome.	Random Urine	2 working days (samples received Wed/Sat by 9 AM)	950.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Serotonin (5-hydroxytryptamine) levels", "Neuroendocrine activity"] Parameters [{"name": "Serotonin (5-HT)", "reference_range": null}] Preparation ["Avoid bananas, walnuts, tomatoes, pineapples, plums, gooseberries, mirabelles, melons, avocados, aubergines, kiwi fruits for 48 hours prior.", "Avoid methocarbamol, mephenesin, guaifenesin, paracetamol, salicylic acid for 48 hours prior.", "Avoid strenuous exercise for 48 hours prior.", "Collect 50 mL (10 mL min.) random urine.", "Acidify urine to pH 1–2 using 50% HCl dropwise.", "Ship refrigerated or frozen."] Indications ["Suspected neuroendocrine tumours", "Suspected carcinoid syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 3379-3 ICD-10: E34.0 Clinical summary This diagnostic test evaluates the level of serotonin (5-hydroxytryptamine) in a random urine sample to help diagnose neuroendocrine tumours and carcinoid syndrome.
TEST-3108 Serotonin (5‑HT) Serum Test This diagnostic test evaluates the concentration of serotonin in the serum.	Serum	Samples collected by Tuesday 9:00 AM yield results by Friday. General turnaround: 3-4 business days.	750.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Circulating serotonin levels"] Parameters [{"name": "Serotonin (5-HT)", "reference_range": "50–200 ng/mL"}] Preparation ["Strictly avoid bananas, walnuts, tomatoes, pineapples, plums, gooseberries, avocados, aubergines, kiwi fruits, chocolates for 48 hours before collection.", "Avoid drugs like Lithium, MAO Inhibitors, Methyldopa, Reserpine, Fluoxetine for 48 hours before collection.", "Refrain from strenuous exercise 48 hours before and during collection.", "Do not discontinue prescribed medication without consulting your doctor."] Indications ["Diagnosis of carcinoid tumors", "Monitoring of serotonin-secreting malignancies", "Suspected serotonin syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 2711-8 ICD-10: E34.0, C7A.00, D3A.00 Clinical summary This diagnostic test evaluates the concentration of serotonin in the serum.
TEST-4322 SERPIN1 Gene Familial Encephalopathy with Neuroserpin Inclusion Bodies Genetic Test This genetic test evaluates the SERPIN1 gene for pathogenic variants associated with Familial Encephalopathy with Neuroserpin Inclusion Bodies (FENIB).	Peripheral blood (EDTA), dried blood spot (FTA card), or extracted genomic DNA	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SERPIN1 gene sequence", "Copy Number Variants (CNVs) in SERPIN1"] Parameters [{"name": "Sensitivity", "reference_range": "99.9% for SERPIN1 pathogenic variants"}, {"name": "Coverage Depth", "reference_range": ">500×"}] Preparation ["No specific fasting required.", "Do not discontinue prescribed medications unless advised by your physician."] Indications ["Suspected diagnosis of Familial Encephalopathy with Neuroserpin Inclusion Bodies (FENIB)", "Family history of FENIB", "Carrier screening in at-risk relatives"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: G31.89, G31.8 Clinical summary This genetic test evaluates the SERPIN1 gene for pathogenic variants associated with Familial Encephalopathy with Neuroserpin Inclusion Bodies (FENIB).
TEST-4105 SERPINC1 Gene Antithrombin III Deficiency Genetic Test This genetic test evaluates the SERPINC1 gene for mutations causing hereditary antithrombin III deficiency.	Whole Blood (Peripheral)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SERPINC1 gene sequence", "Single nucleotide variants", "Small indels", "Copy number variations (CNV)"] Parameters [] Preparation ["Genetic counseling session is mandatory prior to sample collection.", "No specific fasting or medication adjustments are required for the blood draw."] Indications ["Personal or family history of venous thromboembolism (VTE)", "Unexplained recurrent miscarriage", "Pre-surgical risk assessment for thrombophilia", "Evaluation of suspected hereditary antithrombin deficiency"] Measurement technique Confirm with laboratory Codes LOINC: 90368-6 ICD-10: D68.51 Clinical summary This genetic test evaluates the SERPINC1 gene for mutations causing hereditary antithrombin III deficiency.

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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