Rabbit Polyclonal Antibody to UGT8

包装: 1G|100G|500G|1KG|100KG

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别名:2-hydroxyacylsphingosine 1-beta-galactosyltransferase, Ceramide UDP-galactosyltransferase, Cerebroside synthase, UDP-galactose-ceramide galactosyltransferase, UGT8, CGT, UGT4
应用:WB
反应种属:Human, Mouse, Rat
规格：50μl/100μl

Description
Galactocerebrosides are abundant sphingolipids of the myelin membrane of the central nervous system and peripheral nervous system and are also present in small amounts in kidney. The key enzymatic step in the biosynthesis of galactocerebrosides consists of the transfer of galactose to ceramide catalyzed by UDP-galactose ceramide galactosyltransferase (CGT, EC 2.4.1.45). The enzyme encoded by the CGT gene is the first involved in complex lipid biosynthesis in the myelinating oligodendrocyte.[supplied by OMIM].

Description

Galactocerebrosides are abundant sphingolipids of the
myelin membrane of the central nervous system and peripheral
nervous system and are also present in small amounts in kidney. The
key enzymatic step in the biosynthesis of galactocerebrosides
consists of the transfer of galactose to ceramide catalyzed by
UDP-galactose ceramide galactosyltransferase (CGT, EC 2.4.1.45).
The enzyme encoded by the CGT gene is the first involved in complex
lipid biosynthesis in the myelinating oligodendrocyte.[supplied by
OMIM].

Specification
Aliases	2-hydroxyacylsphingosine 1-beta-galactosyltransferase, Ceramide UDP-galactosyltransferase, Cerebroside synthase, UDP-galactose-ceramide galactosyltransferase, UGT8, CGT, UGT4
Entrez GeneID	7368
Swissprot	Q16880
WB Predicted band size	61.4kDa
Host/Isotype	Rabbit IgG
Storage	Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Species Reactivity	Human, Mouse, Rat
Immunogen	This UGT8 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 366-393 amino acids from the Central region of human UGT8.
Formulation	Purified polyclonal antibody supplied in PBS with 0.05% sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.