Background:

This gene encodes a muscle enzyme involved in glycogenolysis. Highly similar enzymes encoded by different genes are found in liver and brain. Mutations in this gene are associated with McArdle disease (myophosphorylase deficiency)| a glycogen storage disease of muscle. Alternative splicing results in multiple transcript variants.

Classification:

Primary antibody

Alternative names:

PYGM

Species reactivity:

Human, Mouse, Rat

Host:

Rabbit

Isotype:

IgG

Immunogen:

Synthesized peptide derived from human PYGM

Concentration:

1 mg/ml

Molecular weight:

92620

Applications:

WB

Storage:

-20°C for 1 year

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