Tianlong Human MTHFR (C677T) Gene Polymorphism Detection Kit

22-11-2022

People with abnormal MTHFR gene have low enzyme activity and folic acid metabolism disorders, which lead to a significantly increased risk of neonatal neural tube defects, down syndrome, and cleft lip and palate. And such people need more folic acid supplements to achieve the desired effect.

 

The most common polymorphism of the MTHFR gene is C677T, which locates in the catalytic domain of MTHFR, and its polymorphism leads to decreased enzyme activity and thermolability.

 

This product is for in vitro qualitative detection of methylenetetrahydrofolate reductase (MTHFR) gene 677 genotype in DNA extracted from human peripheral blood. Therefore, the test results of this kit provide an auxiliary diagnosis for high-risk groups with low activity of methylenetetrahydrofolate reductase.

 

Reliable Detection: Reliable detection of methylenetetrahydrofolate reductase (MTHFR) gene 677 genotype, the most common polymorphism of the MTHFR gene

 

High Sensitivity: Sensitive to detect up to 2ng/μL human genomic DNA

 

More Accessible: CE marked, accessible for more countries


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