ST3GAL5 anticorps

N° du produit ABIN2855684

L’anticorps Lapin Polyclonal anti-ST3GAL5 a été validé pour WB. Il convient pour détecter ST3GAL5 dans des échantillons de Humain.

Aperçu rapide pour ST3GAL5 anticorps (ABIN2855684)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ST3GAL5 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-ST3GAL5 anticorps

Réactivité croisée: Humain

Attributs du produit: Rabbit Polyclonal antibody to ST3GAL5 (ST3 beta-galactoside alpha-2,3-sialyltransferase 5)
ST3GAL5 antibody

Purification: Purified by antigen-affinity chromatography.

Immunogène: Recombinant protein encompassing a sequence within the center region of human ST3GAL5. The exact sequence is proprietary.

Isotype: IgG

Information d'application

Indications d'application: WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Commentaires:

Positive Control: U87-MG

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: 1XPBS ( pH 7), 20 % Glycerol, 0.01 % Thimerosal

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Détails sur ST3GAL5

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

Autre désignation: ST3 beta-galactoside alpha-2,3-sialyltransferase 5

Sujet: 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.

Cellular Localization: Golgi apparatus membrane, Single-pass type II membrane protein

Poids moléculaire: 48 kDa

ID gène: 8869

UniProt: Q9UNP4