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.

Applications:

ELISA, WB, IHC

Name of antibody:

PYGM

Immunogen:

Fusion protein of human PYGM

Full name:

phosphorylase, glycogen, muscle

SwissProt:

P11217

ELISA Recommended dilution:

2000-5000

IHC positive control:

Human thyroid cancer and Human liver cancer

IHC Recommend dilution:

30-150

WB Predicted band size:

97 kDa

WB Positive control:

Mouse heart tissue

WB Recommended dilution:

500-2000