Showing 785–800 of 1143 results
The Metanephrines Normetanephrines (24 Hour Urine) test is the specialized diagnostic tool designed to catch this invisible storm.
Sample Type : 24 Hour Urine
Methodology : HPLC – High Performance Liquid Chromatography
TAT : 10 Days
The Methadone Urine Test is the tool that ensures you stay on the right side of that line. It isn’t about policing you; it is about protecting your recovery and your health.
Sample Type : Random Urine
Methodology : Immunochromatography
TAT : 1 Day
Sample Type : Whole Blood
Methodology : PCR-RFLP
TAT : 15 Days
Sample Type : 24 Hour Urine
Methodology : Immunoturbidometry
TAT : 1 Day
Sample Type : Random Urine
Methodology : Immunoturbidometry
TAT : 1 Day
Sample Type : Random or 24 hrs Urine collection
Methodology : Spectrophotometry
TAT : 1 Day
Sample Type : Random Urine/Serum
Methodology : Spectrophotometry
TAT : 1 Day
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.
Sample Type : Serum
Methodology : Haemagglutination (HA)
TAT : 1 Day
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.
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.
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.
Sample Type : Whole Blood
Methodology : “Direct Mutation Analysis by PCR, & Mutation Detection Enhancement (MDE)”
TAT : 15 Days