ST3GAL5 antibody

Catalog No. ABIN5966528

Product Details anti-ST3GAL5 Antibody

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

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This ST3GAL5 antibody is un-conjugated

Application: Western Blotting (WB)

Purification: Affinity purification

Immunogen: Recombinant protein of human ST3GAL5

Isotype: IgG

Application Details

Application Notes: WB 1:500 - 1:2000

Restrictions: For Research Use only

Handling

Concentration: 1 mg/mL

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

Preservative: Sodium azide

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

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for ST3GAL5

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

Alternative Name: ST3GAL5 (ST3GAL5 Products)

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

Background:

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.

Molecular Weight:

Observed_MW: 48kDa

Calculated_MW: 45kDa/47kDa

Gene ID: 8869

UniProt: Q9UNP4