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

Confirm test-specific instructions with your clinician or laboratory.

Compare available tests

Biochemistry test prices

Showing 91–105 of 1,113 matching tests.

Biochemistry diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-207 Amitriptyline Test This test measures the concentration of amitriptyline and its active metabolite nortriptyline in the serum.	Serum	2–3 weeks (specimens received by the 7th of the month)	2,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Serum Amitriptyline", "Serum Nortriptyline"] Parameters [{"name": "Amitriptyline", "reference_range": null}, {"name": "Nortriptyline", "reference_range": null}] Preparation ["Collect blood sample exactly 12 hours after the last oral dose.", "Ensure patient is at steady-state (usually after 5–7 days of consistent dosing).", "Use a plain red-top tube without gel separator.", "Do not stop or alter medication without medical advice.", "Sign the mandatory Form 35 consent at the time of collection."] Indications ["Monitoring therapeutic drug levels", "Optimising dosage for depression, neuropathic pain, or migraine prophylaxis", "Assessing patient compliance", "Investigating suspected toxicity or side effects"] Measurement technique Confirm with laboratory Codes LOINC: 3471-2 ICD-10: Z51.81 Clinical summary This test measures the concentration of amitriptyline and its active metabolite nortriptyline in the serum.
TEST-5234 AMPD1 Gene Myopathy (Myoadenylate Deaminase Deficiency) Genetic Test This genetic test identifies pathogenic variants in the AMPD1 gene associated with myoadenylate deaminase deficiency.	Peripheral Whole Blood (EDTA) or Dried Blood Spot (DBS)	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 AMPD1 gene", "Genetic predisposition to myoadenylate deaminase deficiency"] Parameters [] Preparation ["No specific fasting required", "Avoid recent blood transfusions (within 2 weeks)"] Indications ["Diagnostic confirmation of suspected myoadenylate deaminase deficiency", "Family screening for individuals with a family history of the condition", "Evaluation of unexplained exercise intolerance or rhabdomyolysis"] Measurement technique Confirm with laboratory Codes LOINC: 51956-7 ICD-10: E79.2, Z15.89, Z13.79 Clinical summary This genetic test identifies pathogenic variants in the AMPD1 gene associated with myoadenylate deaminase deficiency.
TEST-5516 AMPD2 Gene Sequencing for Pontocerebellar Hypoplasia Type 9 Test This test identifies pathogenic variants in the AMPD2 gene associated with pontocerebellar hypoplasia type 9.	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 AMPD2 gene", "Single nucleotide variants", "Small insertions and deletions", "Copy number alterations"] Parameters [] Preparation [] Indications ["Diagnosis of pontocerebellar hypoplasia type 9", "Carrier testing in at-risk families"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: G31.89 Clinical summary This test identifies pathogenic variants in the AMPD2 gene associated with pontocerebellar hypoplasia type 9.
TEST-5801 AMPD2 Gene SPG63 Genetic Test This test detects pathogenic variants in the AMPD2 gene associated with Hereditary Spastic Paraplegia Type 63 (SPG63).	Peripheral whole blood (EDTA) or extracted genomic DNA	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 AMPD2 gene", "Point mutations", "Small insertions/deletions", "Copy number variations"] Parameters [] Preparation [] Indications ["Clinical suspicion of Hereditary Spastic Paraplegia Type 63 (SPG63)", "Family history of SPG63", "Neurological examination findings consistent with SPG63"] Measurement technique Confirm with laboratory Codes LOINC: 95035-9 ICD-10: G11.4 Clinical summary This test detects pathogenic variants in the AMPD2 gene associated with Hereditary Spastic Paraplegia Type 63 (SPG63).
TEST-219 Amylase Isoenzymes Test This diagnostic test evaluates the specific types of amylase (pancreatic and salivary) in the blood.	Serum	14–21 Business Days	1,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pancreatic isoamylase (P-type)", "Salivary isoamylase (S-type)"] Parameters [{"name": "Pancreatic Isoamylase", "reference_range": null}, {"name": "Salivary Isoamylase", "reference_range": null}] Preparation ["No fasting is required", "Do not discontinue prescribed medication without consulting your doctor", "Ensure adequate hydration prior to blood draw", "Sign the mandatory Form 35 (Send Out Consent)"] Indications ["Suspected acute pancreatitis", "Evaluation of elevated total amylase", "Differentiation of pancreatic vs. non-pancreatic causes of hyperamylasemia"] Measurement technique Confirm with laboratory Codes LOINC: 1799-9 ICD-10: R74.8 Clinical summary This diagnostic test evaluates the specific types of amylase (pancreatic and salivary) in the blood.
TEST-245 Andrology Panel Test This test evaluates male reproductive and endocrine function by measuring key hormones.	Serum / Plasma	Same Day (Sample received by 9:00 AM)	550.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Total Testosterone", "Free Testosterone", "Luteinizing Hormone (LH)", "Follicle-Stimulating Hormone (FSH)", "Prolactin", "Estradiol", "Sex Hormone-Binding Globulin (SHBG)"] Parameters [{"name": "Total Testosterone", "reference_range": null}, {"name": "Free Testosterone", "reference_range": null}, {"name": "Luteinizing Hormone (LH)", "reference_range": null}, {"name": "Follicle-Stimulating Hormone (FSH)", "reference_range": null}, {"name": "Prolactin", "reference_range": null}, {"name": "Estradiol", "reference_range": null}, {"name": "Sex Hormone-Binding Globulin (SHBG)", "reference_range": null}] Preparation ["Fasting for 8–12 hours is recommended.", "Sample collection between 7:00 AM and 10:00 AM is ideal.", "Avoid vigorous exercise and alcohol consumption for 24 hours prior to testing."] Indications ["Diagnosis of hypogonadism", "Evaluation of male infertility", "Assessment of pituitary disorders", "Investigation of age-related androgen decline"] Measurement technique Confirm with laboratory Codes LOINC: 35558-0 ICD-10: E29.1, R86.2, N46 Clinical summary This test evaluates male reproductive and endocrine function by measuring key hormones.
TEST-246 Androstenedione Serum Test This diagnostic test evaluates circulating levels of androstenedione, a key androgen precursor, to aid in diagnosing adrenal and gonadal disorders.	Serum	Same Day (Mon/Thu before 11 AM)	450.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Circulating androstenedione", "Adrenal and gonadal androgen production"] Parameters [{"name": "Androstenedione", "reference_range": "Adult Male: 0.6–3.1 ng/mL; Premenopausal Female: 0.3–3.3 ng/mL; Postmenopausal Female: 0.2–1.7 ng/mL"}, {"name": "Precision (CV%)", "reference_range": "≤ 3.5% Intra-Assay (CLIA, ISO-Calibrated)"}] Preparation ["Fasting for 8–10 hours (water permitted)", "Avoid strenuous exercise for 24 hours", "Refrain from alcohol consumption for 48 hours", "Inform phlebotomist of all medications, particularly corticosteroids, oral contraceptives, anti-androgens, and hormonal supplements"] Indications ["Diagnosing adrenal disorders", "Diagnosing congenital adrenal hyperplasia (CAH)", "Diagnosing polycystic ovary syndrome (PCOS)", "Diagnosing androgen-secreting tumors", "Evaluating hyperandrogenism", "Evaluating precocious puberty", "Evaluating delayed puberty", "Suspected enzymatic deficiencies in steroidogenesis pathways"] Measurement technique Confirm with laboratory Codes LOINC: 1854-9 ICD-10: E27.8, E25.0, Z13.29 Clinical summary This diagnostic test evaluates circulating levels of androstenedione, a key androgen precursor, to aid in diagnosing adrenal and gonadal disorders.
TEST-249 Androstenedione Stimulation by ACTH Test This diagnostic test evaluates the adrenal gland's functional reserve by measuring the androstenedione response to synthetic ACTH stimulation.	Serum	Same-day (samples received by 4 PM Mon/Thu)	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Androstenedione levels (baseline and post-stimulation)", "Adrenal gland response to ACTH"] Parameters [{"name": "Androstenedione", "reference_range": null}] Preparation ["Overnight fasting (8–12 hours)", "Inform doctor about all medications"] Indications ["Suspected adrenal insufficiency", "Diagnosis of congenital adrenal hyperplasia", "Evaluation of steroidogenesis disorders"] Measurement technique Confirm with laboratory Codes LOINC: 2142-3 ICD-10: E27.4, E25.0 Clinical summary This diagnostic test evaluates the adrenal gland's functional reserve by measuring the androstenedione response to synthetic ACTH stimulation.
TEST-3817 ANG Gene Amyotrophic Lateral Sclerosis Type 9 Genetic Test This test evaluates the angiogenin (ANG) gene for pathogenic variants associated with Amyotrophic Lateral Sclerosis Type 9 (ALS9).	Peripheral whole blood (EDTA) or extracted DNA	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 ANG gene", "Copy number variants (CNVs) in the ANG gene"] Parameters [] Preparation [] Indications ["Individuals presenting with progressive motor weakness", "Individuals with a family history suggestive of ALS type 9"] Measurement technique Confirm with laboratory Codes LOINC: 77772-5 ICD-10: G12.21 Clinical summary This test evaluates the angiogenin (ANG) gene for pathogenic variants associated with Amyotrophic Lateral Sclerosis Type 9 (ALS9).
TEST-262 Angiotensin II (Ang II) Test This diagnostic test evaluates the level of active Angiotensin II in EDTA plasma, a key component of the renin-angiotensin-aldosterone system (RAAS). It aids in the classification...	EDTA Plasma	2-3 weeks (batch-processed; sample must be collected by the 7th of the month)	1,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Active Angiotensin II peptide", "Renin-Angiotensin-Aldosterone System (RAAS) activity"] Parameters [] Preparation ["May require fasting for 8-12 hours", "Be in a seated, rested position for 15 minutes before venipuncture", "Certain antihypertensives may need a supervised pause"] Indications ["Classification of hypertensive disorders", "Guiding targeted therapy for hypertension", "Evaluation of RAAS activity"] Measurement technique Confirm with laboratory Codes LOINC: 2143-9 ICD-10: I15.0, I10 Clinical summary This diagnostic test evaluates the level of active Angiotensin II in EDTA plasma, a key component of the renin-angiotensin-aldosterone system (RAAS). It aids in the classification of hypertensive disorders and guides targeted therapy.
TEST-3178 ANKRD26 Gene Thrombocytopenia Type 2 Genetic Test This genetic test detects pathogenic variants in the ANKRD26 gene associated with inherited thrombocytopenia type 2 (THC2), a bleeding disorder.	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 ANKRD26 gene", "Point mutations", "Small insertions and deletions", "Copy number changes"] Parameters [] Preparation ["No fasting required", "Pre-test genetic counselling is mandatory"] Indications ["Suspected inherited thrombocytopenia type 2", "Family history of low platelet counts or bleeding disorders", "Confirmation of diagnosis in symptomatic individuals", "Predictive testing for at-risk family members"] Measurement technique Confirm with laboratory Codes LOINC: 21673-3 ICD-10: D69.4 Clinical summary This genetic test detects pathogenic variants in the ANKRD26 gene associated with inherited thrombocytopenia type 2 (THC2), a bleeding disorder.
TEST-3656 ANKS6 Gene Nephronophthisis Type 16 Genetic Test This genetic test identifies pathogenic variants in the ANKS6 gene associated with Nephronophthisis Type 16, a form of juvenile cystic kidney disease.	Whole Blood, Extracted DNA, 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 ANKS6 gene"] Parameters [] Preparation ["No fasting required"] Indications ["Suspected Nephronophthisis Type 16", "Family history of juvenile cystic kidney disease", "Early diagnosis of renal disease"] Measurement technique Confirm with laboratory Codes LOINC: 97728-8 ICD-10: Q61.5 Clinical summary This genetic test identifies pathogenic variants in the ANKS6 gene associated with Nephronophthisis Type 16, a form of juvenile cystic kidney disease.
TEST-2080 ANTXR1 Gene Hemangioma Capillary Infantile Genetic Test (NGS) This test evaluates the ANTXR1 gene for pathogenic variants associated with capillary infantile hemangioma.	Peripheral whole blood, extracted DNA, 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 ANTXR1 gene", "Insertions", "Deletions", "Splice-site alterations"] Parameters [] Preparation [] Indications ["Diagnosis of capillary infantile hemangioma", "Genetic counseling for families with ANTXR1-related syndromes"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Q82.8 Clinical summary This test evaluates the ANTXR1 gene for pathogenic variants associated with capillary infantile hemangioma.
TEST-6183 AP2S1 Gene Familial Hypocalciuric Hypercalcemia Type 3 Genetic Test This genetic test analyzes the AP2S1 gene for mutations causing Familial Hypocalciuric Hypercalcemia Type 3 (FHH3). It helps differentiate FHH3 from primary hyperparathyroidism.	Whole blood (EDTA), extracted DNA, 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 AP2S1 gene", "Full exon and splice-site coverage"] Parameters [] Preparation ["No specific fasting required", "Inform lab of recent blood transfusions (within 4 weeks)"] Indications ["Diagnosis of FHH3", "Family cascade screening for FHH3", "Differentiation from primary hyperparathyroidism"] Measurement technique Confirm with laboratory Codes LOINC: 94492-9 ICD-10: ['E83.52', 'E83.51', 'Z13.79'] Clinical summary This genetic test analyzes the AP2S1 gene for mutations causing Familial Hypocalciuric Hypercalcemia Type 3 (FHH3). It helps differentiate FHH3 from primary hyperparathyroidism.
TEST-5668 AP4B1 Gene (SPG47) Next-Generation Sequencing (NGS) Genetic Test This test identifies mutations in the AP4B1 gene associated with Hereditary Spastic Paraplegia Type 47 (SPG47).	Whole blood (3–5 mL in EDTA tube), pre-extracted genomic DNA (≥1 µg at ≥50 ng/µL), or dried blood spot on 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 ["AP4B1 gene coding sequence", "Pathogenic point mutations", "Small insertions/deletions", "Copy number variations"] Parameters [] Preparation ["No fasting or special preparation needed"] Indications ["Diagnosis of Hereditary Spastic Paraplegia Type 47 (SPG47)", "Patients with clinical features suggestive of SPG47"] Measurement technique Confirm with laboratory Codes LOINC: 94243-0 ICD-10: G11.4 Clinical summary This test identifies mutations in the AP4B1 gene associated with Hereditary Spastic Paraplegia Type 47 (SPG47).

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.

Before booking

Use the test details as a conversation starter

The right diagnostic option depends on your reason for testing and individual circumstances. Check the listed specimen and timing, then confirm any preparation requirements with the ordering clinician or laboratory before collection.

Explore this area

Biochemistry tests in Dubai & UAE

Biochemistry test prices

Biochemistry: overview

Use the test details as a conversation starter

Related Biochemistry categories