Showing 1–16 of 32 results
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3.500,00 د.إThe 24G DNA Ancestry Test offers a comprehensive analysis of your genetic heritage, tracing your ancestry across 2,400+ global regions with high precision. Utilizing cutting-edge genomic technology, it provides deep insights into your ethnic composition, migration patterns, and ancestral connections. The test also includes maternal and paternal lineage tracing (mtDNA & Y-DNA for males), helping you uncover ancient origins. Unlike standard ancestry tests, 24G DNA delivers high-resolution regional breakdowns, historical insights, and potential relative matching, making it a powerful tool for exploring your genetic past.
Sample Type : Saliva
Methodology : Illumina
TAT : 3-6 Weeks
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3.500,00 د.إThe 24G Health DNA Test is a comprehensive genetic test that analyzes 24 key health-related genes to provide personalized insights into your wellness, nutrition, fitness, and disease risk. It offers actionable recommendations tailored to your DNA, helping you optimize your lifestyle, diet, and exercise routines.
Sample Type : Saliva
Methodology : Illumina
TAT : 3-6 Weeks
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3.500,00 د.إThe 24G Pharmacogenomics plus DNA Test is a cutting-edge genetic analysis that provides personalized insights into drug response and overall health. It examines pharmacogenomics, helping to predict how your body metabolizes medications, reducing adverse drug reactions and optimizing treatment plans. Additionally, it includes a comprehensive DNA test covering traits, wellness, and genetic predispositions. Key benefits include personalized medication guidance, enhanced treatment safety, and actionable health insights.
Sample Type : Saliva
Methodology : Illumina
TAT : 3-6 Weeks
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1.650,00 د.إAdenovirus DNA, Quantitative Real-Time PCR is a highly sensitive and specific molecular diagnostic test designed for the rapid and accurate quantification of adenovirus DNA in clinical samples. Utilizing real-time PCR technology, it ensures precise viral load measurement, enabling early detection and effective monitoring of infections.
Sample Type : Stool
Methodology : Real-time PCR
TAT : 10 Days
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3.300,00 د.إALK Fusion – FISH is a fluorescence in situ hybridization (FISH) test designed to detect ALK gene rearrangements in tumor samples, primarily for non-small cell lung cancer (NSCLC) patients. Key features include high sensitivity and specificity, FDA approval for clinical diagnostics, and direct visualization of ALK gene fusions at the cellular level.
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2.150,00 د.إThe Amniotic Fluid Karyotype Test detects chromosomal abnormalities like Down syndrome. Accurate results in 30 days. Book your prenatal test with Lab Tests Dubai.
Sample Type : Amiotic Fluid
Methodology : Conventional Cytogenetics: Culture + Chromosome analysis
TAT : 30 Days
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1.250,00 د.إThe Bacterial Vaginosis DNA, Quant, RT-PCR test is an advanced molecular diagnostic tool designed for the accurate detection and quantification of bacterial vaginosis (BV)-associated pathogens. Utilizing real-time PCR (RT-PCR) technology, it provides rapid, precise, and quantitative analysis of key bacterial species linked to BV, including Gardnerella vaginalis, Atopobium vaginae, and others.
Sample Type : Vaginal Swab
Methodology : Real-time polymerase chain reaction (PCR)
TAT : 3 Days
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3.250,00 د.إThe BCR/ABL – Quantitative test is a highly sensitive molecular diagnostic assay used to detect and quantify the BCR-ABL fusion gene, a key biomarker in chronic myeloid leukemia (CML) and some acute lymphoblastic leukemias (ALL). Utilizing real-time PCR technology, it provides precise measurement of BCR-ABL transcript levels, enabling accurate disease monitoring and treatment response assessment.
Sample Type : Whole Blood
Methodology : Real time PCR
TAT : 8-10 Days
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3.950,00 د.إBeta Thalassemia by PCR is a molecular diagnostic test designed to detect mutations in the HBB gene responsible for beta thalassemia.
Sample Type : EDTA Whole Blood
Methodology : PCR
TAT : 4 Weeks
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9.120,00 د.إSample Type : EDTA blood
Methodology : NGS
TAT : 15 Days
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2.150,00 د.إSample Type : Whole Blood
Methodology : Conventional Cytogenetics: Culture + Chromosome analysis
TAT : 30 Days
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4.000,00 د.إThe NGS Colorectal Cancer Panel from Lab Tests Dubai is a state-of-the-art genetic test that decodes the unique mutations in your tumor, unlocking critical insights for personalized treatment, targeted therapy selection, and hereditary risk assessment.
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3.400,00 د.إThe Fragile X (FMR1) Mutation Screen (L) is a genetic test designed to detect mutations in the FMR1 gene, which are associated with Fragile X syndrome, a leading cause of inherited intellectual disability and autism. This screening identifies CGG repeat expansions, distinguishing between normal, premutation, and full mutation alleles. Key benefits include early detection for informed reproductive decisions, risk assessment for carriers, and guidance for personalized medical management. Utilizing advanced molecular techniques, the test ensures high accuracy and reliability. Ideal for individuals with a family history of Fragile X or unexplained developmental delays, this screening provides critical genetic insights for proactive healthcare planning.
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6.250,00 د.إDetect Fragile-X Syndrome with a lab test that identifies FMR1 gene mutations linked to intellectual disability and developmental delays.
Sample Type : Whole Blood
Methodology : Direct Mutation Analysis by PCR and Southern Blot Analysis
TAT : 30 Days
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2.820,00 د.إThe HER-2/NEU – FISH Test is a highly precise diagnostic tool used to detect HER-2 gene amplification in breast cancer and other malignancies. Utilizing Fluorescence In Situ Hybridization (FISH) technology, it provides accurate, reliable, and early detection of HER-2 status, which is crucial for determining targeted therapy eligibility, such as Herceptin (trastuzumab) treatment.
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4.000,00 د.إThe **Hereditary Cancer Gene Panel (57 ACMG Genes)** is a comprehensive genetic test designed to assess inherited cancer risk by analyzing 57 clinically significant genes recommended by the **American College of Medical Genetics (ACMG)**. This panel identifies mutations linked to various hereditary cancers, including **breast, ovarian, colorectal, prostate, and pancreatic cancers**, enabling early detection and personalized risk management. Key features include **next-generation sequencing (NGS) technology** for high accuracy, expert-reviewed results, and actionable insights for **preventive care and targeted treatment strategies**. Ideal for individuals with a family history of cancer, this test empowers proactive healthcare decisions, offering **lifelong benefits through early intervention and precision medicine**.
