MTHFR C677T Mutation Detection Kit
£326.00
The MTHFR C677T Mutation Detection Kit is designed for the identification of the MTHFR C677T mutation, a genetic variant associated with an increased susceptibility to thrombosis, particularly when combined with other risk factors. Utilizing multiplex RT-PCR technology, this kit simplifies the process of detecting this specific mutation, aiding in the assessment of thrombophilia risk and coagulation abnormalities.
- Ready to Reaction Mix: Simplifies the test setup, making it user-friendly for laboratory personnel.
- Accurate Results: Includes controls for both homozygous and heterozygous mutations to ensure the reliability of test outcomes.
- Dual Color Compatibility: Compatible with real-time PCR instruments that detect FAM and VIC/HEX, allowing for the simultaneous detection of multiple genetic risk factors.
- CE-IVD Certification: Adheres to European standards for in vitro diagnostic medical devices, ensuring the kit’s quality and dependability.
Genetic Risk Assessment for Thrombophilia: Targeted towards the detection of the MTHFR C677T mutation, this kit serves as a valuable tool for evaluating genetic predispositions to thrombophilia and related vascular disorders, including venous thrombosis and pulmonary embolism.
- Technology: Employs multiplex RT-PCR for the targeted detection of the MTHFR C677T mutation, alongside other thrombophilia-related genetic risk factors.
- Compatibility: Compatible with FAM and VIC/HEX dual-color real-time PCR instruments.
- Controls Included: Features controls for both homozygous and heterozygous conditions to validate assay accuracy.
- Certification: Carries the CE-IVD marking, indicating its suitability for in vitro diagnostic use within the European Union.
Why Choose Clent
We strive to enable our customers to focus on the results of their work, rather than the tools they use. Need to speak with a member of our team? Get in touch today.
