Dubai Lab Tests Top Services
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| Thumbnails | Products | Price | Quantity | Action | |
|---|---|---|---|---|---|
 | AED1,600.00 | ||||
| MTHFR C677T Gene Mutation Test – DNA Analysis for Genetic Health Insights The MTHFR Mutation (C677T) Analysis is a genetic test that identifies the presence of the C677T variant in the MTHFR gene, which can impact folate metabolism and homocysteine levels. Key features include accurate DNA analysis using a simple saliva or cheek swab sample, fast turnaround time, and clear, actionable results. Benefits include personalized insights into potential health risks such as cardiovascular issues, fertility challenges, and neurological conditions, enabling targeted lifestyle and nutritional interventions. Its unique selling point lies in empowering individuals with genetic knowledge to make informed health decisions and optimize wellness through precision nutrition. | AED1,600.00 | |||
 | MTHFR C677T & A1298C Genetic Mutation Test – DNA Analysis for Methylation & Health Insights The MTHFR C677T & A1298C Detection Lab Test isa genetic screening tool that identifies mutations in the MTHFR gene, which can impact folate metabolism, homocysteine levels, and overall health. Key features include accurate detection of both common MTHFR variants (C677T and A1298C) through a simple saliva or blood sample. | AED1,000.00 | |||
| Prothrombin Mutation Analysis – Accurate DNA Analysis for Thrombophilia Detection The Prothrombin Mutation Analysis is a genetic test designed to detect the G20210A mutation in the prothrombin (F2) gene, a key risk factor for inherited thrombophilia. This highly accurate, DNA-based assay identifies individuals with increased risk of abnormal blood clotting, aiding in the diagnosis and management of thrombotic disorders. | AED2,400.00 | |||
 | MTRR A66G Genetic Test – Personalized Health & Methylation Analysis The MTRR A66G test is a genetic screening tool that identifies a specific variant (A66G) in the MTRR gene, which plays a crucial role in folate metabolism and homocysteine regulation. Key features include accurate DNA analysis, easy sample collection (typically via saliva or cheek swab), and fast turnaround time. | AED1,520.00 | |||
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| AED3,200.00 | ||||
 | Life Geno DNA Wellness Test – Comprehensive Genetic Health & Fitness Screening Panel The Life Geno-DNA Based Comprehensive Wellness Screening Panel is an advanced genetic testing solution that analyzes your DNA to provide personalized insights into your overall health, wellness, and disease risk. Key features include in-depth analysis of genetic markers related to nutrition, fitness, metabolism, sleep, stress, and predisposition to chronic conditions. | AED3,750.00 | |||
 | Y Chromosome Microdeletion Test for Men – Accurate Male Infertility Screening The Y Chromosome Microdeletion (YCMD) Blood Test is a specialized genetic screening designed exclusively for males to detect microdeletions in the Y chromosome, a key factor in male infertility. This test identifies deletions in the AZF (Azoospermia Factor) regions, which are crucial for sperm production. | AED2,800.00 | |||
 | Mitochondrial DNA Sequencing | High-Accuracy mtDNA Analysis for Research & Medicine Mitochondrial DNA (mtDNA) Sequencing provides high-resolution analysis of mitochondrial genomes, enabling precise identification of genetic variations. Key features include full-length mtDNA sequencing, high accuracy, and deep coverage, ensuring reliable detection of mutations and heteroplasmy. Benefits include applications in ancestry research, forensic identification, disease association studies, and evolutionary biology. | AED3,750.00 | |||
 | Whole Exome Sequencing Whole Exome Sequencing (WES) isa powerful genetic testing method that sequences all protein-coding regions (exons) of the genome, covering approximately 1-2% of the DNA where most disease-causing mutations occur. It offers a cost-effective alternative to whole genome sequencing while providing high-depth coverage for accurate variant detection. WES enables the identification of genetic mutations linked to inherited disorders, cancer, and rare diseases, making it a valuable tool for clinical diagnostics, personalized medicine, and research. | AED5,375.00 | |||
 | ALK Fusion – FISH ALK 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. | AED3,300.00 | |||
 | ROS1 FISH Test – Accurate Genetic Testing for Targeted Cancer Therapy The **Ros1 – Fish Test** is a highly sensitive and reliable fluorescence in situ hybridization (FISH) assay designed for the detection of **ROS1 gene rearrangements** in tumor samples. This test is crucial for identifying patients who may benefit from targeted therapies, particularly in **non-small cell lung cancer (NSCLC)**. Key features include **high specificity and accuracy**, rapid turnaround time, and **direct visualization of gene rearrangements** at the cellular level. Its benefits include **early and precise diagnosis**, enabling personalized treatment decisions and improving patient outcomes. The **unique selling point** of the Ros1 – Fish Test is its **proven clinical utility in guiding targeted therapy selection**, making it an essential tool for oncologists and pathologists in precision medicine. | AED3,750.00 | |||
 | PD-L1 (22C3) Dako CPS IHC Test – Accurate Immunohistochemistry for Cancer Diagnosis The PD-L1 (22C3) Dako CPS (IHC) test is an immunohistochemistry (IHC) assay designed to assess PD-L1 expression in tumor and immune cells using the Combined Positive Score (CPS). It isFDA-approved as a companion diagnostic for multiple cancer therapies, ensuring precise patient selection for immune checkpoint inhibitors. The test utilizes the 22C3 monoclonal antibody, providing high sensitivity and specificity in detecting PD-L1 expression. Its standardized scoring system (CPS) enhances reproducibility and clinical decision-making, making it a trusted tool for oncologists. The Dako platform ensures consistent, high-quality staining, supporting accurate and reliable results for personalized cancer treatment. | AED3,500.00 | |||
 | HER-2/NEU – FISH Test The 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. This test offers higher sensitivity and specificity compared to immunohistochemistry (IHC), reducing false-positive or false-negative results. Its rapid turnaround time and clinically validated methodology make it a gold standard for personalized cancer treatment, ensuring optimal therapeutic decisions and improved patient outcomes. | AED2,820.00 | |||
 | Oncotype DX Breast Cancer Test – Personalized Risk Assessment & Treatment Guidance The Oncotype DX Breast Cancer (ML) Test is a genomic assay that analyzes the activity of 21 genes in a breast cancer tumor to predict the risk of recurrence and the potential benefit of chemotherapy. Designed for early-stage, hormone receptor-positive, HER2-negative breast cancer patients, it provides a Recurrence Score® result that helps guide personalized treatment decisions. Key benefits include reducing unnecessary chemotherapy, improving patient outcomes, and offering evidence-based insights backed by extensive clinical validation. | AED35,000.00 | |||
 | Karyotyping – Products Of Conception (L) Unlock critical genetic insights with **Karyotyping – Products of Conception (L)**, a specialized diagnostic test designed to analyze chromosomal abnormalities in fetal tissue following pregnancy loss. This advanced cytogenetic analysis provides essential information to help identify potential genetic causes of miscarriage, offering valuable guidance for future reproductive planning. | AED2,400.00 | |||
 | PCR FOR HLA B27 (EDTA) PCR for HLA-B27 (EDTA) is a molecular diagnostic test used to detect the HLA-B27 gene, which is strongly associated with autoimmune disorders like ankylosing spondylitis and other spondyloarthropathies. Utilizing Polymerase Chain Reaction (PCR) technology, this test offers high sensitivity and specificity, ensuring accurate and reliable results. The use of EDTA as an anticoagulant preserves sample integrity, enhancing test precision. Key benefits include early disease detection, aiding in timely diagnosis and management of autoimmune conditions. Its rapid turnaround time and non-invasive nature make it a preferred choice for clinicians. | AED2,400.00 |