購物車
幫助
021-54845833/15800441009
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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] |
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Applications: |
WB, IHC |
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Name of antibody: |
PYGM |
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Immunogen: |
Fusion protein of human PYGM |
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Full name: |
glycogen phosphorylase, muscle associated |
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SwissProt: |
P11217 |
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IHC positive control: |
Human adult heart tissue |
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IHC Recommend dilution: |
500-2000 |
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WB Predicted band size: |
97 KD |
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WB Positive control: |
PC12, HepG2, RAW264.7, NIH/3T3 cell lysates |
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WB Recommended dilution: |
500-2000 |
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