Showing 28–36 of 65 results
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AED2,720.00
The Jak 2 Exon 12-15 Mutation Analysis is a specialized genetic test designed to detect mutations in exons 12-15 of the JAK2 gene, which are associated with myeloproliferative neoplasms (MPNs) such as polycythemia vera (PV) and other hematologic disorders. This test offers high sensitivity and specificity, enabling early and accurate diagnosis, which is crucial for targeted treatment decisions and disease monitoring. Unlike standard JAK2 V617F mutation tests, this analysis identifies rare but clinically significant mutations, providing comprehensive genetic profiling for patients with suspected MPNs. Its advanced molecular technology ensures reliable results, supporting personalized therapeutic strategies and improving patient outcomes.
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AED2,400.00
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.
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AED3,750.00
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.
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AED3,750.00
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.
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AED1,000.00
The MTHFR C677T & A1298C Detection Lab Test is a 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.
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AED1,600.00
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.
