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 226–240 of 1,113 matching tests.

Biochemistry diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-3914 CLCNKA Gene Sequencing for Bartter Syndrome Type 4B (Genetic Test) This test identifies pathogenic variants in the CLCNKA gene associated with Bartter syndrome type 4B.	Whole Blood (EDTA) or 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 ["CLCNKA gene sequence", "Pathogenic variants"] Parameters [] Preparation ["Avoid blood transfusion for 90 days prior", "Bring detailed clinical history", "Arrange for genetic counsellor consultation"] Indications ["Clinical suspicion of Bartter syndrome", "Family history of Bartter syndrome", "Unexplained electrolyte imbalances"] Measurement technique Confirm with laboratory Codes LOINC: 94257-2 ICD-10: E26.81, Z84.81, Z14.8 Clinical summary This test identifies pathogenic variants in the CLCNKA gene associated with Bartter syndrome type 4B.
TEST-6092 CLN8 Gene Neuronal Ceroid Lipofuscinosis Type 8 (NCL8) Genetic Test This genetic test evaluates the CLN8 gene for pathogenic variants associated with Neuronal Ceroid Lipofuscinosis type 8 (NCL8).	Whole Blood (EDTA), Extracted DNA, or FTA Card Dried Blood Spot	21–28 Business Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the CLN8 gene", "Single nucleotide variants", "Small insertions/deletions", "Copy number variations"] Parameters [] Preparation ["Mandatory pre-test genetic counselling session", "Review of relevant neurology reports, MRI findings, and prior genetic test results"] Indications ["Suspected diagnosis of NCL8", "Carrier screening", "Family planning", "Genetic confirmation"] Measurement technique Confirm with laboratory Codes LOINC: 94233-3 ICD-10: E75.4 Clinical summary This genetic test evaluates the CLN8 gene for pathogenic variants associated with Neuronal Ceroid Lipofuscinosis type 8 (NCL8).
TEST-665 Clomipramine (Anafranil) Therapeutic Drug Monitoring Test This diagnostic test evaluates the concentration of clomipramine in the patient's serum. It aids in assessing medication efficacy and potential toxicity.	Serum	2-3 weeks (monthly batch; cut-off 7th of month)	1,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Serum Clomipramine Concentration"] Parameters [{"name": "Clomipramine", "reference_range": null}] Preparation ["Collect a 4 mL serum sample in a plain red-top tube", "Sample collection at least 12 hours after the last oral dose", "Arrange refrigerated transport with home phlebotomy team"] Indications ["Optimizing clomipramine dosage", "Assessing therapeutic drug levels", "Monitoring for toxicity", "Evaluating patient adherence"] Measurement technique Confirm with laboratory Codes LOINC: 3530-0 ICD-10: Z51.81 Clinical summary This diagnostic test evaluates the concentration of clomipramine in the patient's serum. It aids in assessing medication efficacy and potential toxicity.
TEST-669 Clonazepam Test This test measures the concentration of clonazepam in the serum to monitor therapeutic levels and guide dosage adjustments.	Serum	2-3 weeks (sample cut-off: 7th of each month)	1,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Serum Clonazepam Concentration"] Parameters [{"name": "Clonazepam", "reference_range": null}] Preparation ["Collect blood before the next dose (trough level)", "Use a plain red-top tube without gel", "Ship refrigerated (2-8°C)", "No special fasting required", "Avoid SST gel-barrier tubes", "Sign the mandatory Send-Out Consent Form (Form 35)"] Indications ["Therapeutic drug monitoring for anxiety, panic, and epilepsy", "Dose adjustment", "Assessment of adherence", "Investigation of suspected toxicity or side effects"] Measurement technique Confirm with laboratory Codes LOINC: 4011-2 ICD-10: Z79.899 Clinical summary This test measures the concentration of clonazepam in the serum to monitor therapeutic levels and guide dosage adjustments.
TEST-673 Clorazepate Test This diagnostic test quantifies the concentration of clorazepate and its active metabolite nordazepam in serum.	Serum	2–3 weeks	2,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Clorazepate", "Nordazepam"] Parameters [{"name": "Clorazepate", "reference_range": null}, {"name": "Nordazepam", "reference_range": null}] Preparation ["Schedule blood draw immediately before next scheduled dose (trough level)", "Fast for at least 6 hours prior", "Avoid alcohol for 24 hours", "Inform phlebotomist of all medications, supplements, and grapefruit consumption"] Indications ["Monitoring therapeutic levels in patients on clorazepate", "Guiding dose adjustments", "Preventing toxicity", "Assessing adherence"] Measurement technique Confirm with laboratory Codes LOINC: 39437-5 ICD-10: Z51.81 Clinical summary This diagnostic test quantifies the concentration of clorazepate and its active metabolite nordazepam in serum.
TEST-676 Clozapine Therapeutic Drug Monitoring Test This test quantitatively measures serum concentrations of clozapine and its active metabolite norclozapine.	Serum	2–3 weeks (sample must arrive by the 7th of the month)	1,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Serum Clozapine", "Serum Norclozapine"] Parameters [{"name": "Clozapine", "reference_range": "350–600 ng/mL"}, {"name": "Norclozapine", "reference_range": null}] Preparation ["Blood must be drawn as a trough sample, precisely 0.5 to 1 hour before the next scheduled oral dose at steady state.", "Requires 2 mL of serum collected in a plain Red Top tube (no SST gel barrier tubes)."] Indications ["Therapeutic dose optimization for treatment-resistant schizophrenia", "Toxicity prevention", "Monitoring patients with variable metabolism", "Assessing adherence"] Measurement technique Confirm with laboratory Codes LOINC: 3585-4 ICD-10: Z51.81 Clinical summary This test quantitatively measures serum concentrations of clozapine and its active metabolite norclozapine.
TEST-6168 CNNM2 Gene Hypomagnesemia Type 6 Genetic Test This test detects pathogenic variants in the CNNM2 gene associated with Hypomagnesemia Type 6, a rare autosomal dominant disorder affecting magnesium metabolism.	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 CNNM2 gene", "Zygosity of variants"] Parameters [] Preparation ["No fasting required", "No medication adjustments required", "Pre-test genetic counselling is mandatory"] Indications ["Individuals and families with a history of magnesium metabolism disorders", "Diagnosis of Hypomagnesemia Type 6"] Measurement technique Confirm with laboratory Codes LOINC: 82319-8 ICD-10: E83.42 Clinical summary This test detects pathogenic variants in the CNNM2 gene associated with Hypomagnesemia Type 6, a rare autosomal dominant disorder affecting magnesium metabolism.
TEST-4090 CNTN1 Gene Genetic Test (Compton-North Congenital Myopathy) This test identifies pathogenic variants in the CNTN1 gene, confirming the genetic basis for Compton-North congenital myopathy.	Peripheral whole blood (3–5 mL in EDTA tube)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CNTN1 gene coding region variants", "Pathogenic mutations"] Parameters [] Preparation ["Inform team of recent blood transfusion or stem cell transplant", "Reschedule if febrile >38.5°C"] Indications ["Suspected Compton-North congenital myopathy", "Family history of congenital myopathy", "Need for definitive molecular diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 56267-3 ICD-10: G71.2 Clinical summary This test identifies pathogenic variants in the CNTN1 gene, confirming the genetic basis for Compton-North congenital myopathy.
TEST-4150 CNTNAP2 Gene Cortical Dysplasia-Focal Epilepsy Syndrome Genetic Test This test identifies pathogenic variants within the CNTNAP2 gene associated with cortical dysplasia-focal epilepsy syndrome.	Peripheral blood (3–5 mL EDTA), FTA card spot, or extracted DNA (≥1 µg)	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 CNTNAP2 gene", "Deep intronic variants", "Copy-number variants"] Parameters [] Preparation ["Pre-test genetic counselling session mandatory", "Detailed pedigree documentation required"] Indications ["Diagnosis of cortical dysplasia-focal epilepsy syndrome", "Genetic counselling for affected families"] Measurement technique Confirm with laboratory Codes LOINC: 78025-5 ICD-10: Q04.3, G40.0 Clinical summary This test identifies pathogenic variants within the CNTNAP2 gene associated with cortical dysplasia-focal epilepsy syndrome.
TEST-687 Cobalt 24-Hour Urine Test This diagnostic test evaluates recent cobalt exposure and the body's ability to excrete it.	24-Hour Urine	Next day (sample received by 6:00 PM)	650.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Cobalt concentration in urine", "Body's excretion capacity"] Parameters [{"name": "Cobalt", "reference_range": null}] Preparation ["Stop mineral supplements, Vitamin B12, and Vitamin B Complex 3 days prior.", "Avoid Gadolinium or Iodine contrast media 96 hours prior.", "Use only the metal-free container kit provided.", "Wear powder-less gloves during collection.", "Record total 24-hour urine volume."] Indications ["Suspected industrial cobalt toxicity", "Monitoring occupational exposure", "Guiding detoxification protocols"] Measurement technique Confirm with laboratory Codes LOINC: 14949-2 ICD-10: Z77.021 Clinical summary This diagnostic test evaluates recent cobalt exposure and the body's ability to excrete it.
TEST-689 Cobalt Blood Test This diagnostic test evaluates the concentration of cobalt in whole blood.	Whole Blood	Next-day report (sample by 6 pm)	650.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Cobalt concentration", "Heavy metal levels"] Parameters [{"name": "Cobalt", "reference_range": null}] Preparation ["Withhold mineral supplements, vitamin B12, and B-complex for 3 days prior (if clinically safe)", "Wait 96 hours after Gadolinium or Iodine contrast imaging"] Indications ["Suspected occupational exposure", "Prosthetic joint wear monitoring", "Investigation of systemic toxicity"] Measurement technique Confirm with laboratory Codes LOINC: 5681-7 ICD-10: T56.0 Clinical summary This diagnostic test evaluates the concentration of cobalt in whole blood.
TEST-684 Cobalt, Random Urine Test This test measures the concentration of cobalt in a random urine sample to assess recent exposure to the metal.	Random urine (mid-stream, 10 mL)	Next-day report (sample received by 6 PM)	650.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Cobalt concentration in urine"] Parameters [{"name": "Cobalt", "reference_range": null}] Preparation ["Stop all mineral supplements, vitamin B12, and vitamin B complex at least three days prior.", "Avoid contrast media for 96 hours before collection.", "Consult your doctor before stopping any prescribed medication."] Indications ["Assessment of occupational or environmental cobalt exposure", "Monitoring chelation therapy", "Investigation of suspected cobalt toxicity"] Measurement technique Confirm with laboratory Codes LOINC: 5686-2 ICD-10: Z77.018 Clinical summary This test measures the concentration of cobalt in a random urine sample to assess recent exposure to the metal.
TEST-5669 COCH Gene Deafness, Autosomal Dominant Type 9 Genetic Test This test identifies pathogenic variants in the COCH gene associated with autosomal dominant non-syndromic hearing loss type 9 (DFNA9). It uses Next Generation Sequencing (NGS) for...	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 COCH gene", "Exons and splice-site junctions of the COCH gene"] Parameters [] Preparation ["No fasting required", "No special dietary restrictions", "Pre-genetic counselling session recommended"] Indications ["Clinical suspicion of DFNA9", "Adults with post-lingual hearing loss", "Family history of hereditary hearing loss"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: H90.3 Clinical summary This test identifies pathogenic variants in the COCH gene associated with autosomal dominant non-syndromic hearing loss type 9 (DFNA9). It uses Next Generation Sequencing (NGS) for comprehensive analysis.
TEST-4553 COG1 Gene Glycosylation Disorder Type 2g (CDG-2g) Genetic Test This genetic test identifies pathogenic variants in the COG1 gene associated with congenital disorder of glycosylation type IIg.	Peripheral whole blood (EDTA) or Dry 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 COG1 gene", "Single nucleotide variants (SNVs)", "Insertions/deletions (indels)", "Copy number variants (CNVs)"] Parameters [] Preparation ["Do not discontinue prescribed medication without consulting your physician."] Indications ["Diagnosis of congenital disorder of glycosylation type IIg (CDG-2g)", "Evaluation of patients with suspected neurometabolic disorders"] Measurement technique Confirm with laboratory Codes LOINC: 81247-4 ICD-10: E77.8 Clinical summary This genetic test identifies pathogenic variants in the COG1 gene associated with congenital disorder of glycosylation type IIg.
TEST-6272 COG5 Gene Glycosylation Disorder Type 2I Genetic Test This test analyzes the COG5 gene for pathogenic variants associated with Congenital Disorder of Glycosylation type IIi (CDG-2I). It uses Next Generation Sequencing (NGS) for compre...	Peripheral whole blood (EDTA), 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 ["Pathogenic variants in the COG5 gene", "Congenital Disorder of Glycosylation type IIi (CDG-2I)"] Parameters [] Preparation [] Indications ["Suspected Congenital Disorder of Glycosylation type IIi (CDG-2I)", "Family history of COG5-related disease"] Measurement technique Confirm with laboratory Codes LOINC: 83240-0 ICD-10: E77.8 Clinical summary This test analyzes the COG5 gene for pathogenic variants associated with Congenital Disorder of Glycosylation type IIi (CDG-2I). It uses Next Generation Sequencing (NGS) for comprehensive analysis.

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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