PHKG2 anticorps

N° du produit ABIN7117512

Cet anticorps anti-PHKG2 est un anticorps Lapin Polyclonal détectant PHKG2 dans WB, IHC et ELISA. Adapté pour Humain, Souris et Rat.

Aperçu rapide pour PHKG2 anticorps (ABIN7117512)

Antigène: PHKG2 (phosphorylase Kinase, gamma 2 (Testis) (PHKG2))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PHKG2 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), ELISA

Détail du produit anti-PHKG2 anticorps

Fonction: PHKG2 antibody

Purification: Immunogen affinity purified

Pureté: ≥95 % as determined by SDS-PAGE

Immunogène: phosphorylase kinase, gamma 2 (testis)

Isotype: IgG

Information d'application

Indications d'application: WB: 1:500 - 1:2000, IHC: 1:50 - 1:100

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Conseil sur la manipulation: Avoid repeated freeze / thaw cycles.

Stock: -20 °C

Stockage commentaire: -20°C for 12 months

Date de péremption: 12 months

Détails sur PHKG2

Antigène: PHKG2 (phosphorylase Kinase, gamma 2 (Testis) (PHKG2))

Autre désignation: PHKG2

Sujet:

Synonyms: Phosphorylase b kinase gamma catalytic chain, liver/testis isoform (PHK-gamma-LT, PHK-gamma-T)|PSK-C3|Phosphorylase kinase subunit gamma-2|PHKG2

Background: Phosphorylase kinase is a polymer of 16 subunits, four each of alpha, beta, gamma and delta. The alpha subunit includes the skeletal muscle and hepatic isoforms, encoded by two different genes. The beta subunit is the same in both the muscle and hepatic isoforms, and encoded by one gene. The gamma subunit also includes the skeletal muscle and hepatic isoforms, and the hepatic isoform is encoded by this gene. The delta subunit is a calmodulin and can be encoded by three different genes. The gamma subunits contain the active site of the enzyme, whereas the alpha and beta subunits have regulatory functions controlled by phosphorylation. The delta subunit mediates the dependence of the enzyme on calcium concentration. Mutations in this gene cause glycogen storage disease type 9C, also known as autosomal liver glycogenosis. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.

Poids moléculaire: 46 kDa

ID gène: 5261

UniProt: P15735

Pathways: Cellular Glucan Metabolic Process, Regulation of Carbohydrate Metabolic Process