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 |