MTHFR A1298C Mutation Detection Kit
£326.00
The MTHFR A1298C Mutation Detection Kit is designed to identify the MTHFR A1298C mutation, alongside the MTHFR C677T variant, to assess compound heterozygosity—a condition associated with an increased risk of cardiovascular disease. Leveraging multiplex RT-PCR technology, this kit facilitates the detection of these genetic factors that contribute to abnormal blood coagulation and thrombosis risk.
- Ready to Reaction Mix: Offers a streamlined, user-friendly testing process by minimizing preparation steps.
- Accurate Results: Includes both homozygous and heterozygous controls to ensure the reliability and accuracy of test results.
- Dual Color Compatibility: Designed for compatibility with real-time PCR instruments capable of detecting FAM and VIC/HEX, allowing for the simultaneous detection of multiple mutations.
- CE-IVD Certification: Meets European standards for in vitro diagnostic medical devices, ensuring the kit’s quality and reliability.
Genetic Risk Assessment for Cardiovascular Disease: Primarily used to detect the presence of the MTHFR A1298C mutation and compound heterozygosity with MTHFR C677T, this kit is crucial for evaluating the genetic predisposition to cardiovascular diseases and thrombophilia.
- Technology: Utilizes multiplex RT-PCR for the targeted detection of the MTHFR C677T and A1298C mutations, among other genetic risk factors for thrombophilia.
- Compatibility: Suitable for FAM and VIC/HEX dual-color real-time PCR instruments.
- Controls Included: Features controls for both homozygous and heterozygous conditions to ensure testing accuracy.
- Certification: Carries the CE-IVD marking, indicating its approved use within the European Union for in vitro diagnostics.
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