VCAN c.5808T>C

VCAN c.5808T>C

The VCAN c.5808T>C Novallele Genotyping Assay identifies a single nucleotide change of the VCAN gene. The VCAN gene encodes for a protein involved in cell adhesion, proliferation, migration, and angiogenesis. Research has shown mutations in the VCAN gene may be associated with Wagner syndrome type 1.


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Product Description

The VCAN c.5808T>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 necessary for PCR and subsequent allele identification by DNA melting. For Research Use Only. Not for use in diagnostic procedures.