Glycogen Synthase anticorps

N° du produit ABIN265444

Détail du produit anti-Glycogen Synthase anticorps

Antigène: Glycogen Synthase (GYS)

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Glycogen Synthase est non-conjugé

Application: Western Blotting (WB)

Specificité: This antibody detects endogenous levels of Glycogen Synthase protein. (region surrounding Pro539)

Réactivité croisée (Details): Species reactivity (expected):Mouse and Rat.
Species reactivity (tested):Human.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen

Pureté: > 95 % pure by SDS-PAGE

Information d'application

Indications d'application: ELISA: 1: 5000approx. 1: 20000. WB: 1: 500approx. 1: 1000.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user.

Restrictions: For Research Use only

Stockage

Concentration: 1.0 mg/mL

Buffer: Phosphate buffered saline (PBS), pH 7.2., 15 mM sodium azide

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: DO NOT FREEZE!

Stock: 4 °C

Stockage commentaire: Store the antibody undiluted at 2-8 °C.

Détails sur Glycogen Synthase

Antigène: Glycogen Synthase (GYS)

Autre désignation: Glycogen Synthase (GYS Produits)

Synonymes: anticorps CG6940, anticorps Dmel\\CG6904, anticorps anon-WO0118547.108, anticorps glycogen synthase, anticorps Glycogen synthase, anticorps starch synthase, anticorps glgA, anticorps GlyS, anticorps glgA-2, anticorps glgA-1, anticorps EAMY_RS33325, anticorps Hipma_0956, anticorps Tresu_1353, anticorps Spico_0935, anticorps Trebr_1511, anticorps Mahau_1987

Sujet: Glycogen (starch) synthase belongs to the mammalian/fungal glycogen synthase family of proteins. Two forms of this protein exist, a liver form and a muscle form, both of which have the same function in the glycogen biosynthesis pathway. Glycogen synthase transfers the glycosyl residue from UDP-glucose to the nonreducing end of α-1,4-glucan. The 81 kDa liver glycogen synthase protein is truncated by 34 amino acids compared to the muscle form. However, these enzymes differ significantly in their amino- and carboxyl-terminal regions. Muscle glycogen synthase serves to fuel muscular activity only and is regulated by muscle contraction and by catecholamines. Liver glycogen synthase mediates blood glucose homeostasis in response to nutritional cues. Defects in the gene encoding liver glycogen synthase results in glycogen storage disease type 0 (GSD0), a rare form of fasting ketotic hypoglycemia.Synonyms: GYS, GYS1, muscle Glycogen Synthase

Poids moléculaire: approx. 84 kDa

ID gène: 2997

NCBI Accession: NP_001155059

UniProt: P13807