Mouse Glycogen phosphorylase, muscle form (PYGM) ELISA Kit

Mutations in the muscle isoform of glycogen phosphorylase (PYGM) are associated with McArdle disease (glycogen storage disease type V). More than 65 mutations in the PYGM gene that lead to McArdle disease have been identified to date.Gautron et al. (1987) isolated muscle phosphorylase cDNA clones from a human cDNA library. Northern blot experiments revealed 1 specific mRNA of 3.4 kb found uniquely in tissues expressing muscle phosphorylase.\nThe muscle glycogen phosphorylase protein comprises 842 amino acids (Kubisch et al., 1998).Burke et al. (1987) determined the intron/exon structure of the PYGM gene. Kubisch et al. (1998) provided a revised genomic structure for the PYGM gene, which contains 20 exons.

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SPECIFICATIONS

Catalog Number

KTE70590

Size

48T, 96T, 96T*5, 96T*50

Applications

ELISA

Reactivities

Mouse

Gene Id

19309

Accession

Q9WUB3

Additional Info

Mouse Glycogen phosphorylase, muscle form (PYGM) ELISA Kit has high sensitivity and excellent specificity for detection of Mouse PYGM. No significant cross-reactivity or interference between Mouse PYGM and analogues was observed.