ST3GAL5 anticorps

N° du produit ABIN5966528

Détail du produit anti-ST3GAL5 anticorps

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ST3GAL5 est non-conjugé

Application: Western Blotting (WB)

Purification: Affinity purification

Immunogène: Recombinant protein of human ST3GAL5

Isotype: IgG

Information d'application

Indications d'application: WB 1:500 - 1:2000

Restrictions: For Research Use only

Stockage

Concentration: 1 mg/mL

Buffer: Buffer: PBS with 0.02 % sodium azide, 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.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur ST3GAL5

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

Autre désignation: ST3GAL5 (ST3GAL5 Produits)

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

Sujet:

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.

Poids moléculaire:

Observed_MW: 48kDa

Calculated_MW: 45kDa/47kDa

ID gène: 8869

UniProt: Q9UNP4