F13A1 c.103G>T

F13A1 c.103G>T

The F13A1 c.103G>T Novallele Genotyping Assay identifies a single mutation associated with the F13A1 gene. Mutations of this gene are associated with Factor XIII subunit A deficiency. Factor XIII subunit A deficiency is an autosomal recessive hematologic disorder characterized by life-long bleeding tendency, impaired wound healing, and spontaneous abortion in affected women.


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Product Description

The F13A1 c.103G>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.