小鼠抗PYGM单克隆抗体

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.[provided by RefSeq, Sep 2009]

Applications:

WB, IHC

Name of antibody:

PYGM

Immunogen:

Fusion protein of human PYGM

Full name:

glycogen phosphorylase, muscle associated

SwissProt:

P11217

IHC positive control:

Human adult heart tissue

IHC Recommend dilution:

500-2000

WB Predicted band size:

97 KD

WB Positive control:

PC12, HepG2, RAW264.7, NIH/3T3 cell lysates

WB Recommended dilution:

500-2000