PYGM polyclonal, anti-human, mouse, rat

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.

Alternative Name:
Myophosphorylase

Application Dilution: WB: 1:500 - 1:2000

Specificity: PYGM polyclonal antibody detects endogenous levels of PYGM protein.

Immunogen:
A synthetic peptide of human PYGM.

MW: ~ 97 kDa

Swis Prot.: P11217

Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).

Format:
1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.

For research use only, not for use in diagnostic procedure.