FANCC c.67delG

FANCC c.67delG

The FANCC c.67delG Novallele Genotyping Assay identifies a single nucleotide deletion within the FANCC gene. The FANCC gene is associated with the cell process involved in the Fanconi anemia (FA) pathway. Fanconi anemia is characterized by a decrease in bone marrow function, increased cancer and tumor risk, and physical abnormalities.


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Product Description

The FANCC c.67delG 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.