CFH c.1337-7883G>A

CFH c.1337-7883G>A

The CFH c.1337-7883G>A Novallele Genotyping Assay identifies a single nucleotide change of the CFH gene. Research demonstrates that mutations of the CFH gene may cause hemolytic uremic syndrome and complement factor H deficiency. These pathways may be related to cancer and coagulation.


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Product Description

The CFH c.1337-7883G>A 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.