BTD c.1368A>C

BTD c.1368A>C

The BTD c.1368A>C Novallele Genotyping Assay identifies a single nucleotide change of the BTD gene. Mutation of the BTD gene may be linked to biotinidase deficiency. Biotinidase deficiency is characterized by recurring seizures, hypotonia, and infections such as candidiasis.


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Product Description

The BTD c.1368A>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.