ST3GAL5 antibody [N3C3]

Cannot supply to this region.

SKU:: GTX115152
Additional Names:: ST3 beta-galactoside alpha-2,3-sialyltransferase 5 , SATI , SIAT9 , SIATGM3S , SPDRS , ST3Gal V , ST3GalV
Application:: WB, IHC-P
Concentration:: 1.37 mg/ml
Physical State:: Liquid
Species Reactivity:: Human
Purification:: Affinity Purified
Storage Conditions:: -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Supplier:: Genetex
Host:: Rabbit
Reactivities:: Human, Mouse
Buffer:: PBS, 20% Glycerol, 0.025% ProClin 300.
Immunogen:: Recombinant protein encompassing a sequence within the center region of human ST3GAL5. The exact sequence is proprietary.
Clone:: N3C3
Uniprot:: Q9UNP4
Synonyms:: alpha 2,3-sialyltransferase V;CMP-NeuAc:lactosylceramide alpha-2,3-sialyltransferase;ganglioside GM3 synthase;GM3 synthase;lactosylceramide alpha-2,3-sialyltransferase;SATI;Sialyltransferase 9;sialyltransferase 9 (CMP-NeuAc:lactosylceramide alpha-2,3-sialyltransferase; GM3 synthase);SIAT9;SIATGM3S;SPDRS;ST3 beta-galactoside alpha-23-sialyltransferase 5;ST3Gal V;ST3GalV
Extra Details:: 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. [provided by RefSeq]

Shipping Conditions:: Blue Ice