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 136–150 of 1,113 matching tests.

Biochemistry diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-3920 BBS1 Gene Bardet-Biedl Syndrome Type 1 Genetic Test (NGS) This test analyzes the BBS1 gene using Next Generation Sequencing (NGS) to detect pathogenic variants associated with Bardet-Biedl Syndrome Type 1.	Whole Blood (Peripheral) or 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 BBS1 gene", "Missense variants", "Nonsense variants", "Frameshift variants", "Splice-site variants", "Deep intronic variants"] Parameters [] Preparation ["No special dietary or medication preparation is needed", "Continue all prescribed therapies unless advised otherwise by your physician"] Indications ["Suspected Bardet-Biedl Syndrome Type 1", "Family history of Bardet-Biedl Syndrome Type 1", "Need for genetic counselling regarding BBS1-related risks"] Measurement technique Confirm with laboratory Codes LOINC: 94267-3 ICD-10: Q87.8 Clinical summary This test analyzes the BBS1 gene using Next Generation Sequencing (NGS) to detect pathogenic variants associated with Bardet-Biedl Syndrome Type 1.
TEST-3958 BBS12 Gene (Bardet-Biedl Syndrome Type 12) Genetic Test This test identifies pathogenic variants in the BBS12 gene to confirm a diagnosis of Bardet-Biedl syndrome type 12.	Whole Blood (EDTA), Extracted DNA, 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 BBS12 gene"] Parameters [] Preparation ["Fasting is not required", "Pre-test genetic counselling is mandatory"] Indications ["Diagnosis of Bardet-Biedl syndrome type 12", "Carrier detection in at-risk family members", "Prenatal diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 103204-9 ICD-10: Q87.89 Clinical summary This test identifies pathogenic variants in the BBS12 gene to confirm a diagnosis of Bardet-Biedl syndrome type 12.
TEST-3898 BBS5 Gene Bardet-Biedl Syndrome Type 5 Genetic Test This test identifies pathogenic variants in the BBS5 gene associated with Bardet-Biedl syndrome type 5.	Peripheral 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 BBS5 gene", "Single Nucleotide Variants (SNVs)", "Insertions/Deletions (indels)", "Copy Number Variations (CNVs)"] Parameters [] Preparation ["Pre-genetic counselling session required", "Completed clinical history form required"] Indications ["Individuals with suggestive clinical features of Bardet-Biedl syndrome type 5", "Family history of ciliopathies", "Pre-test genetic counseling recommended"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: Q87.89 Clinical summary This test identifies pathogenic variants in the BBS5 gene associated with Bardet-Biedl syndrome type 5.
TEST-6093 BCKDHA Gene Maple Syrup Urine Disease Type 1a Genetic Test This test identifies pathogenic variants in the BCKDHA gene associated with Maple Syrup Urine Disease Type 1a.	Peripheral Whole Blood or FTA Card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["BCKDHA gene pathogenic variants", "Single nucleotide variants", "Small insertions and deletions", "Copy-number changes"] Parameters [] Preparation ["Mandatory pre-test genetic counselling session", "Do not discontinue prescribed medication or initiate a leucine-restricted diet without physician supervision"] Indications ["Suspected Maple Syrup Urine Disease Type 1a", "Carrier screening", "Family cascade screening"] Measurement technique Confirm with laboratory Codes LOINC: 21629-5 ICD-10: E71.0 Clinical summary This test identifies pathogenic variants in the BCKDHA gene associated with Maple Syrup Urine Disease Type 1a.
TEST-6040 BCKDHB Gene Maple Syrup Urine Disease Type 1b Genetic Test This test identifies pathogenic variants in the BCKDHB gene to confirm a diagnosis of Maple Syrup Urine Disease (MSUD) type 1b.	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 BCKDHB gene", "Presence of point mutations, small indels, and CNVs"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed branched-chain amino acid formula or dietary management without consulting a metabolic specialist"] Indications ["Suspected diagnosis of Maple Syrup Urine Disease (MSUD) type 1b", "Differential diagnosis in patients with metabolic acidosis", "Cascade screening for at-risk family members"] Measurement technique Confirm with laboratory Codes LOINC: 21638-3 ICD-10: E71.0 Clinical summary This test identifies pathogenic variants in the BCKDHB gene to confirm a diagnosis of Maple Syrup Urine Disease (MSUD) type 1b.
TEST-6047 BCKDK Gene Genetic Test for Branched-Chain Ketoacid Dehydrogenase Kinase Deficiency This test identifies genetic mutations in the BCKDK gene associated with branched-chain ketoacid dehydrogenase kinase deficiency.	Whole 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 ["BCKDK gene sequence", "Pathogenic variants in BCKDK gene"] Parameters [] Preparation ["Inform laboratory of recent blood transfusion (within 4 weeks)", "Notify phlebotomist if on anticoagulant therapy"] Indications ["Diagnosis of BCKDK deficiency", "Carrier screening", "Prenatal testing", "Family risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 92737-7 ICD-10: E71.1 Clinical summary This test identifies genetic mutations in the BCKDK gene associated with branched-chain ketoacid dehydrogenase kinase deficiency.
TEST-1836 BCL6 Gene Rearrangement (FISH) Test This test detects chromosomal rearrangements of the BCL6 gene using Fluorescence In-Situ Hybridization (FISH). It is a key molecular marker for classifying and understanding B-cell...	Bone marrow aspirate or peripheral whole blood	5–6 working days	900.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["BCL6 gene rearrangements", "Chromosomal translocations at 3q27"] Parameters [] Preparation ["No special fasting required"] Indications ["Classification of B-cell lymphomas", "Prognostic assessment in lymphoma", "Guiding targeted therapy decisions"] Measurement technique Confirm with laboratory Codes LOINC: 49583-7 ICD-10: C83.9 Clinical summary This test detects chromosomal rearrangements of the BCL6 gene using Fluorescence In-Situ Hybridization (FISH). It is a key molecular marker for classifying and understanding B-cell lymphomas.
TEST-5157 BCS1L Gene Mitochondrial Complex III Deficiency Genetic Test This genetic test evaluates the BCS1L gene for pathogenic variants associated with mitochondrial complex III deficiency.	Peripheral whole blood (EDTA) or buccal swab	12–18 Business Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["BCS1L gene coding sequence", "Single-nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Exon-level copy number variants (CNVs)"] Parameters [] Preparation ["A detailed clinical history is required.", "A formal genetic counselling session to draw a pedigree chart is mandatory."] Indications ["Suspected mitochondrial complex III deficiency", "Neonatal-onset encephalopathy", "Hepatopathy", "Renal tubulopathy"] Measurement technique Confirm with laboratory Codes LOINC: 93336-6 ICD-10: E88.49, G31.81 Clinical summary This genetic test evaluates the BCS1L gene for pathogenic variants associated with mitochondrial complex III deficiency.
TEST-398 Beta-2 Transferrin (CSF) Test This diagnostic test specifically identifies the presence of Beta-2 Transferrin, a protein unique to cerebrospinal fluid, in samples other than CSF.	Cerebrospinal Fluid (CSF)	2–3 weeks	7,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Beta-2 Transferrin (desialylated transferrin isoform)", "Presence of CSF in non-CSF samples"] Parameters [] Preparation [] Indications ["Diagnosis of CSF leak", "Differentiation of CSF from other fluids"] Measurement technique Confirm with laboratory Codes LOINC: 4811-3 ICD-10: G96.0 Clinical summary This diagnostic test specifically identifies the presence of Beta-2 Transferrin, a protein unique to cerebrospinal fluid, in samples other than CSF.
TEST-5733 BICD2 Gene Sequencing for Spinal Muscular Atrophy, Lower Extremity, Autosomal Dominant Type 2 (NGS) Test This diagnostic test evaluates the BICD2 gene for pathogenic variants associated with autosomal dominant lower extremity spinal muscular atrophy type 2.	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 ["BICD2 gene sequence", "Pathogenic variants in BICD2"] Parameters [] Preparation ["No special preparation needed"] Indications ["Suspected lower extremity-predominant spinal muscular atrophy type 2", "Family history of autosomal dominant spinal muscular atrophy"] Measurement technique Confirm with laboratory Codes LOINC: 95277-6 ICD-10: G12.1 Clinical summary This diagnostic test evaluates the BICD2 gene for pathogenic variants associated with autosomal dominant lower extremity spinal muscular atrophy type 2.
TEST-412 Biotinidase Activity Quantitative Blood Test This test measures the functional activity of the biotinidase enzyme in serum or plasma to diagnose biotinidase deficiency.	Serum or plasma (peripheral venous blood)	Same day (sample received by 4 pm)	650.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Biotinidase enzyme activity", "Biotin recycling pathway function"] Parameters [{"name": "Biotinidase Activity", "reference_range": "8 - 19 nmol/min/mL"}] Preparation ["No fasting required", "Continue prescribed biotin or multivitamins unless advised otherwise by the physician", "Ensure child is well-hydrated"] Indications ["Newborn screening follow-up", "Suspected biotinidase deficiency based on clinical presentation", "Family history of biotinidase deficiency"] Measurement technique Confirm with laboratory Codes LOINC: 22658-2 ICD-10: E53.8 Clinical summary This test measures the functional activity of the biotinidase enzyme in serum or plasma to diagnose biotinidase deficiency.
TEST-418 Bismuth 24-Hour Urine Test This diagnostic test evaluates the total amount of bismuth excreted in the urine over a 24-hour period.	24-Hour Urine	10–14 Business Days	1,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Total bismuth excretion", "Cumulative exposure to bismuth"] Parameters [{"name": "Bismuth", "reference_range": null}] Preparation ["Avoid all mineral supplements and bismuth-containing products (e.g., Pepto-Bismol) for at least 1 week prior to collection.", "Use only the acid-washed metal-free container provided.", "Do not measure the 24-hour total volume.", "Ship the sample refrigerated or frozen immediately after collection.", "Duly filled Test Send Out Consent Form (Form 35) is mandatory."] Indications ["Occupational health monitoring", "Gastroenterology applications", "Nephrology applications", "Monitoring chelation therapy"] Measurement technique Confirm with laboratory Codes LOINC: 14671-7 ICD-10: T56.891 Clinical summary This diagnostic test evaluates the total amount of bismuth excreted in the urine over a 24-hour period.
TEST-415 Bismuth Random Urine Test This test measures the concentration of bismuth in a random urine sample to assess for potential toxicity.	Random Urine	14–21 calendar days	1,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Bismuth concentration in urine"] Parameters [{"name": "Bismuth", "reference_range": "≤0.1 µg/L"}] Preparation ["Discontinue all bismuth-containing medications (e.g., bismuth subsalicylate) and mineral supplements at least seven days prior to collection.", "Use only the laboratory-supplied acid-washed, metal-free urine container.", "Complete the Test Send Out Consent Form (Form 35) in full before sample pickup."] Indications ["Suspected occupational exposure to bismuth", "Chronic use of bismuth-containing medications", "Assessment of unexplained neurocognitive or renal dysfunction"] Measurement technique Confirm with laboratory Codes LOINC: 5687-2 ICD-10: T56.891 Clinical summary This test measures the concentration of bismuth in a random urine sample to assess for potential toxicity.
TEST-3343 BLNK Gene Agammaglobulinemia Type 4 (Autosomal Recessive) Genetic Test This genetic test identifies pathogenic mutations in the BLNK gene associated with autosomal recessive agammaglobulinemia.	Blood (EDTA), Extracted DNA, or One Drop 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 ["BLNK gene sequence", "Pathogenic mutations in BLNK gene"] Parameters [] Preparation [] Indications ["Suspected autosomal recessive agammaglobulinemia", "Recurrent sinopulmonary infections", "Pan-hypogammaglobulinemia with absent B cells", "Carrier screening in affected families", "Preimplantation genetic testing guidance"] Measurement technique Confirm with laboratory Codes LOINC: 94853-7 ICD-10: D80.0 Clinical summary This genetic test identifies pathogenic mutations in the BLNK gene associated with autosomal recessive agammaglobulinemia.
TEST-4724 BMP1 Gene Osteogenesis Imperfecta Type 13 Genetic Test This test evaluates the BMP1 gene for pathogenic variants associated with Osteogenesis Imperfecta Type 13.	Peripheral Whole Blood or Sterile DNA FTA Card	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["BMP1 gene pathogenic variants", "Single nucleotide variants", "Small insertions/deletions", "Copy number changes"] Parameters [] Preparation [] Indications ["Suspected Osteogenesis Imperfecta Type 13", "Differentiation from other collagenopathies", "Genetic skeletal disorder diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 93025-1 ICD-10: Q78.0 Clinical summary This test evaluates the BMP1 gene for pathogenic variants associated with Osteogenesis Imperfecta Type 13.

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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