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PYGM Antibody

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.

Alternative Name(s)

glycogen muscle; Glycogen phosphorylase, muscle form; GPMM; muscle (McArdle syndrome); muscle glycogen phosphorylase; Myophosphorylase; Phosphorylase glycogen; Phosphorylase, glycogen; muscle (McArdle syndrome); AI115133; Muscpho; PG; PYGM;

Application

WB, IP

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UNIprot

F1MJ28, P11217

clonality

Monoclonal

reactivity

Cow, Human, Mouse, Rat

Research area

Others

source

Mouse

storage

Store at -20 ℃. Stable for 12 months from date of receipt.

PYGM Antibody

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