MTHFR c.1286A>C

MTHFR c.1286A>C

The MTHFR c.1286A>C Novallele Genotyping Assay identifies a single mutation that is associated with methylenetetrahydrofolate reductase (MTHFR) gene. This specific mutation in association with MTHFR c.1286A>C mutation is linked to an increased risk for several types of brain cancer. Mutations of the MTHFG gene may cause a deficiency in methylenetetrahydrofolate, which is characterized by homocystinuria, neural tube defects like anencephaly and spina bifida, and hypertension.


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Product Description

The MTHFR c.1286A>C Novallele Genotyping Assay is used to amplify and identify specific genetic polymorphisms or mutations. This assay provides scientists with a simple way to quickly genotype this locus from isolated human genomic DNA. The assay contains functionally-verified oligonucleotide primers and unlabeled probes necessary for PCR and subsequent allele identification by DNA melting. For Research Use Only. Not for use in diagnostic procedures.