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For reconstitution, we recommend adding 100 µL distilled water to a final antibody concentration of about 1 mg/mL. To use this carrier-free antibody for conjugation experiments, we strongly recommend performing another round of desalting. (Zeba Spin Desalting Columns, 7KMWCO, 0.5 mL, Product # 89882)
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: glycogen muscle; Glycogen phosphorylase, muscle form; GPMM; muscle (McArdle syndrome); muscle glycogen phosphorylase; Myophosphorylase; Phosphorylase glycogen; Phosphorylase, glycogen; muscle (McArdle syndrome)
Gene Aliases: AI115133; Muscpho; PG; PYGM
UniProt ID: (Human) P11217, (Mouse) Q9WUB3
Entrez Gene ID: (Human) 5837, (Rat) 24701, (Mouse) 19309
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