購物車
幫助
021-54845833/15800441009
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Fusion protein corresponding to C terminal 250 amino acids of human PYGM |
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Full name: |
phosphorylase, glycogen, muscle |
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Swissprot: |
P11217 |
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Gene Accession: |
BC126392 |
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Purity: |
>85%, as determined by Coomassie blue stained SDS-PAGE |
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Expression system: |
Escherichia coli |
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Tags: |
His tag C-Terminus, GST tag N-Terminus |
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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. |
