"PYGM" Related Products


Recombinant Human Phosphorylase, Glycogen, Muscle

Cat. No. : PYGM-58H
Product Overview : Recombinant Human Glycogen Phosphorylase produced inE.Coliis a single, non-glycosylated, polypeptide chain having a molecular mass of 97 kDa. The GPBB is purified by proprietary chromatographic techniques.
Description : Glycogen phosphorylase is one of the phosphorylase enzymes (EC It breaks up glycogen into glucose subunits. Glycogen is left with one less glucose molecule, and the free glucose molecule is in the form of glucose-1-phosphate. In order to be used for metabolism, it must be converted to glucose-6-phosphate by the enzyme phosphoglucomutase. Glycogen phosphorylase can only act on linear chains of glycogen (a 1-4 glycosidic linkage). Its work will immediately come to a halt four residues away from a 1-6 branch (which are exceedingly common in glycogen). In these situations, a debranching enzyme is necessary, which will straighten out the chain in that area. Additionally, an alpha 1-6 glucosidase enzyme is required to break the remaining 1-6 residue that remains in the new linear chain. After all this is done, glycogen phosphorylase can continue.
Source : Escherichia Coli.
Physical Appearance : Sterile Filtered colourless liquid formualtion.
Purity : Greater than 85.0% as determined by: (a) Analysis by RP-HPLC. (b) Analysis by SDS-PAGE.
Formulation : 0.8 mg/1ml, each mg of protein contains 50% glycerol.
Applications : Immunoassays and western blot.
Stability : GPBB although stable at 10°C for 7 days, should be stored desiccated below -18°C. Please prevent freeze-thaw cycles.
Gene Name : PYGM phosphorylase, glycogen, muscle [ Homo sapiens ]
Synonyms : PYGM; phosphorylase, glycogen, muscle; McArdle syndrome; glycogen storage disease type V; Glycogen phosphorylase, muscle form;Myophosphorylase; EC; myophosphorylase; muscle glycogen phosphorylase; phosphorylase, glycogen; muscle (McArdle syndrome, glycogen storage disease type V)
Gene ID : 5837
mRNA Refseq : NM_001164716
Protein Refseq : NP_001158188
MIM : 608455
UniProt ID : P11217
Chromosome Location : 11q12-q13.2
Pathway : Insulin signaling pathway; Starch and sucrose metabolism; Metabolism of carbohydrates
Function : AMP binding; drug binding; glycogen phosphorylase activity; nucleotide binding; protein binding; pyridoxal phosphate binding; sugar binding; transferase activity, transferring glycosyl groups

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