ST3GAL5 Antikörper

Produktnummer ABIN5966528

Produktdetails anti-ST3GAL5 Antikörper

Target: ST3GAL5 (ST3 beta-Galactoside alpha-2,3-Sialyltransferase 5 (ST3GAL5))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ST3GAL5 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Aufreinigung: Affinity purification

Immunogen: Recombinant protein of human ST3GAL5

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500 - 1:2000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 1 mg/mL

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

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu ST3GAL5

Target: ST3GAL5 (ST3 beta-Galactoside alpha-2,3-Sialyltransferase 5 (ST3GAL5))

Andere Bezeichnung: ST3GAL5 (ST3GAL5 Produkte)

Synonyme: SATI antikoerper, SIAT9 antikoerper, SIATGM3S antikoerper, ST3GalV antikoerper, ST3GAL-V antikoerper, 3S-T antikoerper, Siat9 antikoerper, [a]2 antikoerper, ST3 beta-galactoside alpha-2,3-sialyltransferase 5 antikoerper, ST3GAL5 antikoerper, St3gal5 antikoerper

Hintergrund:

Synonyms: 3-sialyltransferase,CMP-NeuAc:lactosylceramide alpha-2,CMP-NeuAc:lactosylceramide alpha-2,3-sialyltransferase,EC 2.4.99.9,Ganglioside GM3 synthase,Lactosylceramide alpha-2,3-sialyltransferase,Sialyltransferase 9,SIAT9,SIAT9,SIATGM3S,ST3 beta-galactoside alpha-2,3-sialyltransferase 5,ST3GAL,ST3Gal V,ST3GAL5,ST3GalV

Background: Ganglioside GM3 is known to participate in the induction of cell differentiation, modulation of cell proliferation, maintenance of fibroblast morphology, signal transduction, and integrin-mediated cell adhesion. The protein encoded by this gene is a type II membrane protein which catalyzes the formation of GM3 using lactosylceramide as the substrate. The encoded protein is a member of glycosyltransferase family 29 and may be localized to the Golgi apparatus. Mutation in this gene has been associated with Amish infantile epilepsy syndrome. Transcript variants encoding different isoforms have been found for this gene.

Molekulargewicht:

Observed_MW: 48kDa

Calculated_MW: 45kDa/47kDa

Gen-ID: 8869

UniProt: Q9UNP4