SLC46A1 c.1126C>T

SLC46A1 c.1126C>T

The SLC46A1 c.1126C>T Novallele Genotyping Assay identifies a single nucleotide change of the SLC46A1 gene. The SLC46A1 gene encodes for a proton-coupled folate transporter protein. Research demonstrates that mutations of the SLC46A1 gene may be linked to folate malabsorption and folic acid deficiency anemia.

£177.00

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Product Description

The SLC46A1 c.1126C>T 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.