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 31–45 of 1,113 matching tests.

Biochemistry diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-102 Acetylcholinesterase (AChE) Amniotic Fluid Test This diagnostic test evaluates amniotic fluid for abnormal Acetylcholinesterase (AChE) enzyme isoform patterns, indicating the presence of open neural tube defects.	Amniotic Fluid	14–21 days	1,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Acetylcholinesterase (AChE) enzyme isoform patterns"] Parameters [] Preparation ["No fasting required", "Disclose all current medications, supplements, and history of bleeding disorders to clinician", "Completed consent form (Form 35) required"] Indications ["Pregnancies between 13 and 24 weeks gestation", "Clinical suspicion of open neural tube defect", "Elevated maternal serum alpha-fetoprotein", "Abnormal ultrasound findings"] Measurement technique Confirm with laboratory Codes LOINC: 24468-2 ICD-10: Q05, Q01, Q00 Clinical summary This diagnostic test evaluates amniotic fluid for abnormal Acetylcholinesterase (AChE) enzyme isoform patterns, indicating the presence of open neural tube defects.
TEST-5946 ACHE Gene Acetylcholinesterase Deficiency Genetic Test This test identifies pathogenic variants in the ACHE gene associated with acetylcholinesterase deficiency.	Peripheral whole blood (5 mL EDTA)	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 ACHE gene", "Single-nucleotide variants", "Small insertions/deletions"] Parameters [] Preparation ["No fasting is required", "Inform phlebotomist if taking anticoagulants", "Avoid blood-thinning medications for 24 hours before the draw unless otherwise advised by your doctor"] Indications ["Individuals with a family history of abnormal anaesthesia reactions", "Individuals with unexplained post-operative respiratory failure", "Pre-anaesthetic risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 77607-5 ICD-10: E85.8, Z13.71 Clinical summary This test identifies pathogenic variants in the ACHE gene associated with acetylcholinesterase deficiency.
TEST-3707 ACOX1 Gene (Peroxisomal Acyl-CoA Oxidase Deficiency) Genetic Test This test evaluates the ACOX1 gene for pathogenic variants associated with peroxisomal acyl-CoA oxidase deficiency.	Peripheral Whole Blood	21-28 Working Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the ACOX1 gene", "Single-nucleotide variants", "Small indels", "Copy-number changes"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue anti-epileptic medications or specialized dietary formulas without consultant direction"] Indications ["Suspected peroxisomal acyl-CoA oxidase deficiency", "Severe neurological impairment in infancy"] Measurement technique Confirm with laboratory Codes LOINC: 94541-6 ICD-10: E71.510 Clinical summary This test evaluates the ACOX1 gene for pathogenic variants associated with peroxisomal acyl-CoA oxidase deficiency.
TEST-6105 ACP2 Gene Lysosomal Acid Phosphatase Deficiency Genetic Test This genetic test evaluates the ACP2 gene for mutations associated with lysosomal acid phosphatase deficiency.	Whole blood	3–4 weeks from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ACP2 gene mutations", "Point mutations", "Small indels", "Copy-number variations"] Parameters [] Preparation ["Ensure adequate hydration", "Discontinue anticoagulants only under physician guidance", "Pre-test genetic counseling is mandatory"] Indications ["Suspected lysosomal acid phosphatase deficiency", "Family history of the disorder", "Carrier screening in at-risk families"] Measurement technique Confirm with laboratory Codes LOINC: 92851-1 ICD-10: E77.8 Clinical summary This genetic test evaluates the ACP2 gene for mutations associated with lysosomal acid phosphatase deficiency.
TEST-5294 ACTA1 Gene Nemaline Myopathy Type 3 Genetic Test This test evaluates the ACTA1 gene for pathogenic variants associated with nemaline myopathy type 3.	Peripheral Venous Blood (EDTA)	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 ACTA1 gene"] Parameters [] Preparation ["Pre-test genetic counselling session required", "Informed consent required"] Indications ["Unexplained muscle weakness", "Hypotonia", "Family history of congenital myopathies", "Suspected nemaline myopathy type 3"] Measurement technique Confirm with laboratory Codes LOINC: 88554-0 ICD-10: G71.2 Clinical summary This test evaluates the ACTA1 gene for pathogenic variants associated with nemaline myopathy type 3.
TEST-4138 ACTA2 Gene Moyamoya Disease Type 5 Genetic Test This test identifies genetic variants within the ACTA2 gene associated with Moyamoya disease type 5.	Peripheral whole blood	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Single-nucleotide variants in ACTA2 gene", "Small insertions and deletions in ACTA2 gene", "Copy number changes in ACTA2 gene"] Parameters [] Preparation ["Mandatory pre-test genetic counselling session required", "No fasting required", "No medication adjustments needed before blood draw"] Indications ["Symptomatic individuals suspected of Moyamoya disease type 5", "Individuals with a positive family history of ACTA2-related disease", "Presymptomatic family members of affected individuals", "Confirmation of clinical diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 81765-6 ICD-10: I67.5, Q28.8, Z15.89 Clinical summary This test identifies genetic variants within the ACTA2 gene associated with Moyamoya disease type 5.
TEST-3079 ACTB Gene Baraitser-Winter Syndrome Type 1 Genetic Test This genetic test identifies pathogenic variants within the ACTB gene, confirming a diagnosis of Baraitser-Winter syndrome type 1.	Blood (EDTA) or 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 ACTB gene", "Coding exons and flanking intronic regions of ACTB"] Parameters [] Preparation ["No fasting required", "Complete mandatory genetic counselling session", "Inform phlebotomist of all medications and supplements"] Indications ["Suspected Baraitser-Winter syndrome type 1", "Need for definitive molecular diagnosis", "Genetic counselling for families with suspected cases"] Measurement technique Confirm with laboratory Codes LOINC: 96527-2 ICD-10: Q87.8 Clinical summary This genetic test identifies pathogenic variants within the ACTB gene, confirming a diagnosis of Baraitser-Winter syndrome type 1.
TEST-3052 ACTG1 Gene Baraitser‑Winter Syndrome Type 2 Genetic Test This test identifies pathogenic variants in the ACTG1 gene associated with Baraitser‑Winter syndrome type 2.	Whole Blood (Peripheral)	3–4 weeks (stat reporting available)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the ACTG1 gene"] Parameters [] Preparation ["Provide detailed clinical history", "Provide a three-generation pedigree chart"] Indications ["Suspected Baraitser‑Winter syndrome type 2", "Family history of Baraitser‑Winter syndrome type 2"] Measurement technique Confirm with laboratory Codes LOINC: 95075-6 ICD-10: Q87.0 Clinical summary This test identifies pathogenic variants in the ACTG1 gene associated with Baraitser‑Winter syndrome type 2.
TEST-3316 ACTN1 Gene Bleeding Disorder, Platelet-Type 15 Genetic Test This genetic test evaluates the ACTN1 gene for pathogenic variants associated with Platelet-Type 15 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 ACTN1 gene", "Single-nucleotide variants", "Insertions", "Deletions", "Copy number alterations"] Parameters [] Preparation ["No fasting required", "Provide detailed clinical history documenting bleeding symptoms", "Provide a three-generation family pedigree chart", "Provide any prior platelet function test results"] Indications ["Suspected inherited platelet function defect", "Family history of Platelet-Type 15 Bleeding Disorder", "Evaluation of unexplained bleeding"] Measurement technique Confirm with laboratory Codes LOINC: 78041-7 ICD-10: D69.1 Clinical summary This genetic test evaluates the ACTN1 gene for pathogenic variants associated with Platelet-Type 15 Bleeding Disorder.
TEST-110 Acute Kidney Injury (AKI) Panel Test This diagnostic test evaluates kidney function by measuring serum and urine biomarkers associated with acute kidney injury.	Serum & Random Urine	Same day (if sample reaches lab by 4 PM on Mon/Wed/Fri)	1,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Serum creatinine", "Blood urea nitrogen (BUN)", "Cystatin C", "Urine biomarkers (Neutrophil gelatinase-associated lipocalin - NGAL)"] Parameters [{"name": "Serum Creatinine", "reference_range": null}, {"name": "Blood Urea Nitrogen (BUN)", "reference_range": null}, {"name": "Cystatin C", "reference_range": null}, {"name": "Neutrophil Gelatinase-Associated Lipocalin (NGAL)", "reference_range": null}] Preparation ["No fasting required", "Maintain usual hydration"] Indications ["Suspected acute kidney injury", "Monitoring kidney function in critically ill patients", "Distinguishing pre-renal from intrinsic renal injury"] Measurement technique Confirm with laboratory Codes LOINC: 54089-8 ICD-10: N17.9 Clinical summary This diagnostic test evaluates kidney function by measuring serum and urine biomarkers associated with acute kidney injury.
TEST-4588 ADA Gene Severe Combined Immunodeficiency (ADA-SCID) Genetic Test This test identifies genetic mutations in the ADA gene responsible for Severe Combined Immunodeficiency (ADA-SCID). It uses Next-Generation Sequencing (NGS) for comprehensive analy...	Whole Blood (Peripheral)	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 ADA gene", "Single-nucleotide resolution"] Parameters [] Preparation ["Pre-test genetic counseling required", "No specific fasting or medication adjustments needed"] Indications ["Suspected ADA-SCID", "Confirmation of positive newborn screening", "Evaluation of severe immunodeficiency"] Measurement technique Confirm with laboratory Codes LOINC: 21613-5 ICD-10: D81.3 Clinical summary This test identifies genetic mutations in the ADA gene responsible for Severe Combined Immunodeficiency (ADA-SCID). It uses Next-Generation Sequencing (NGS) for comprehensive analysis.
TEST-3975 ADA2 Gene Sequencing for Childhood-Onset Polyarteritis Nodosa Test This test evaluates the entire coding region of the ADA2 gene for mutations associated with DADA2.	Whole Blood (Venipuncture)	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ADA2 gene mutations", "Adenosine deaminase 2 deficiency"] Parameters [] Preparation ["Inform the phlebotomist about current medications.", "Inform the phlebotomist of any bleeding disorder or anticoagulant use."] Indications ["Suspected DADA2", "Childhood-onset polyarteritis nodosa", "Recurrent unexplained fevers", "Family history of DADA2"] Measurement technique Confirm with laboratory Codes LOINC: 95034-2 ICD-10: M30.0 Clinical summary This test evaluates the entire coding region of the ADA2 gene for mutations associated with DADA2.
TEST-5317 ADAM22 Gene Neurodevelopmental Disorder Genetic Test This test detects pathogenic variants in the ADAM22 gene associated with severe neurodevelopmental disorders and early-onset epileptic encephalopathy.	Peripheral Whole Blood (5-10 mL) or Saliva (Oragene DNA Kit)	3-4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ADAM22 gene pathogenic variants (SNVs, indels, CNVs)", "Synaptic function related to ADAM22 protein"] Parameters [] Preparation ["No specific fasting required", "Continue prescribed medications unless advised otherwise by physician"] Indications ["Diagnosis of suspected ADAM22-related disorders", "Evaluation of early-onset epileptic encephalopathy", "Assessment of severe intellectual disability and autism spectrum traits"] Measurement technique Confirm with laboratory Codes LOINC: 101246-3 ICD-10: G40.89, F70-F79, F84.0 Clinical summary This test detects pathogenic variants in the ADAM22 gene associated with severe neurodevelopmental disorders and early-onset epileptic encephalopathy.
TEST-3151 ADAMTS13 Gene Thrombotic Thrombocytopenic Purpura (TTP) Genetic Test This genetic test identifies mutations in the ADAMTS13 gene associated with congenital Thrombotic Thrombocytopenic Purpura (TTP).	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 ["ADAMTS13 gene mutations", "Carrier status for congenital TTP"] Parameters [] Preparation ["No fasting required", "Continue regular medications unless instructed otherwise"] Indications ["Diagnosis of congenital TTP", "Carrier screening", "Family planning"] Measurement technique Confirm with laboratory Codes LOINC: 81311-5 ICD-10: M31.1 Clinical summary This genetic test identifies mutations in the ADAMTS13 gene associated with congenital Thrombotic Thrombocytopenic Purpura (TTP).
TEST-5193 ADAMTS2 Gene Ehlers-Danlos Syndrome Type 7C (Dermatosparaxis) Genetic Test This genetic test analyzes the ADAMTS2 gene for mutations associated with Ehlers-Danlos syndrome type VIIC (dermatosparaxis). It identifies pathogenic variants to confirm diagnosis...	Peripheral whole blood	3–4 Weeks (Rush option available)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ADAMTS2 gene sequence", "Pathogenic variants (mutations)", "Copy Number Variations (CNV)"] Parameters [] Preparation ["No specific fasting required.", "Inform the lab about recent blood transfusions ( Indications ["Clinical suspicion of Ehlers-Danlos syndrome type VIIC (dermatosparaxis)", "Family history of dermatosparaxis", "Need for definitive genetic diagnosis for management and counseling"] Measurement technique Confirm with laboratory Codes LOINC: 81247-7 ICD-10: Q79.6, Z14.01, Z82.79 Clinical summary This genetic test analyzes the ADAMTS2 gene for mutations associated with Ehlers-Danlos syndrome type VIIC (dermatosparaxis). It identifies pathogenic variants to confirm diagnosis and guide patient management.

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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