Search Thermo Fisher Scientific
图: 1 / 1
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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: glycogen muscle; Glycogen phosphorylase, muscle form; GPMM; muscle (McArdle syndrome); muscle glycogen phosphorylase; Myophosphorylase; Phosphorylase glycogen; Phosphorylase, glycogen; muscle (McArdle syndrome)
基因别名: AI115133; Muscpho; PG; PYGM
UniProt ID: (Human) P11217, (Mouse) Q9WUB3
Entrez Gene ID: (Human) 5837, (Rat) 24701, (Mouse) 19309