Glycogen Synthase Antikörper

Produktnummer ABIN265444

Produktdetails anti-Glycogen Synthase Antikörper

Target: Glycogen Synthase (GYS)

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Glycogen Synthase Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

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

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

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

Reinheit: > 95 % pure by SDS-PAGE

Anwendungsinformationen

Applikationshinweise: 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.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 1.0 mg/mL

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

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handhabung: DO NOT FREEZE!

Lagerung: 4 °C

Informationen zur Lagerung: Store the antibody undiluted at 2-8 °C.

Details zu Glycogen Synthase

Target: Glycogen Synthase (GYS)

Andere Bezeichnung: Glycogen Synthase (GYS Produkte)

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

Hintergrund: 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

Molekulargewicht: approx. 84 kDa

Gen-ID: 2997

NCBI Accession: NP_001155059

UniProt: P13807