"PHKG2" Related Products


Recombinant Human PHKG2, GST-tagged, Active

Cat. No.: PHKG2-388H
Product Overview: Recombinant human full-length PHKG2 was expressed by baculovirus inSf9 cellsusing an N-terminal GST tag. MW=70kDa.
Description: PHKG2 is the hepatic and testis isoform of the gamma subunit of phosphorylase kinase. PHKG2 gene contains 10 exons and spans 9.5 kb and maps to chromosome 16p12.1-p11.2. Deficiency of PHK, a regulatory enzyme of glycogen metabolism, is responsible for 25% of all cases of glycogen storage disease and is genetically and clinically heterogeneous. Mutations in the PHKG2 gene lead to autosomal liver-specific PHK deficiency (glycogen storage disease IXc) and an increased risk of cirrhosis and at least 11 PHKG2 mutations have been identified to date.
Source: Sf9 insect cells using baculovirus.
Sequence: Full-length.
Applications: Kinase Assay, Western Blot.
Storage And Stability: Store product at –70°C. For optimal storage, aliquot target into smaller quantities after centrifugation and store at recommended temperature. For most favorable performance, avoid repeated handling and multiple freeze/thaw cycles.
Gene Name: PHKG2 phosphorylase kinase, gamma 2 (testis) [ Homo sapiens ]
Synonyms: PHKG2; phosphorylase kinase, gamma 2 (testis); GSD9C; Phosphorylase b kinase gamma catalytic chain, testis/liver isoform; PHK-gamma-T; EC; Phosphorylase kinase subunit gamma 2; PSK-C3
Gene ID: 5261
mRNA Refseq: NM_000294
Protein Refseq: NP_000285
UniProt ID: P15735
Chromosome Location: 16p11.2
MIM: 172471
Pathway: Calcium signaling pathway; Insulin signaling pathway; Metabolism of carbohydrates
Function: ATP binding; nucleotide binding; protein binding; transferase activity; calmodulin binding; enzyme binding; sphorylase kinase activity; protein serine/threonine kinase activity

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