EVC c.969T>C

EVC c.969T>C

The EVC c.969T>C Novallele Genotyping Assay identifies a single nucleotide change that is associated with the EVC gene. Mutations of the EVC gene cause Ellis-van Creveld syndrome as well as Weyers acrofacial dysostosis. These conditions are characterized by dwarfism, heart defects, and underdeveloped bones.


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Product Description

The EVC c.969T>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.