HFE c.187C>G c.193A>T

HFE c.187C>G c.193A>T

The HFE c.187C>G c.193A>T Novallele Genotyping Assay detects and distinguishes between both the HFE c.187C>G and HFE c.193A>T mutations of the HFE gene. These mutations are associated with heredity type I hemochromatosis, which is linked to disruption of iron regulation throughout the body. Variation in this gene is also characterized by porphyria and X-linked sideroblastic anemia.


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Product Description

The HFE c.187C>G c.193A>T 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.