Use Able AI chat for product recommendations

B3GAT3 Polyclonal antibody, PBS Only

B3GAT3 Polyclonal Antibody for WB, Indirect ELISA
Cat No. 16586-1-PBS

产品说明书

宿主/亚型

Rabbit / IgG

种属反应性

human

应用

WB, Indirect ELISA

Beta-1,3-glucuronyltransferase 3, EC:2.4.1.135, Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 3, GlcAT I, GLCATI

缓冲液配方: 
偶联物:  Unconjugated
规格价格库存


产品信息

16586-1-PBS targets B3GAT3 in WB, Indirect ELISA applications and shows reactivity with human samples.

经测试应用 WB, Indirect ELISA Application Description
经测试反应性 human
免疫原

CatNo: Ag8362

Product name: Recombinant human B3GAT3 protein

Source: e coli.-derived, PET28a

Tag: 6*His

Domain: 1-335 aa of BC007906

Sequence: MKLKLKNVFLAYFLVSIAGLLYALVQLGQPCDCLPPLRAAAEQLRQKDLRISQLQAELRRPPPAPAQPPEPEALPTIYVVTPTYARLVQKAELVRLSQTLSLVPRLHWLLVEDAEGPTPLVSGLLAASGLLFTHLVVLTPKAQRLREGEPGWVHPRGVEQRNKALDWLRGRGGAVGGEKDPPPPGTQGVVYFADDDNTYSRELFEEMRWTRGVSVWPVGLVGGLRFEGPQVQDGRVVGFHTAWEPSRPFPVDMAGFAVALPLLLDKPNAQFDSTAPRGHLESSLLSHLVDPKDLEPRAANCTRVLVWHTRTEKPKMKQEEQLQRQGRGSDPAIEV

种属同源性预测
宿主/亚型 Rabbit / IgG
抗体类别 Polyclonal
产品类型 Antibody
全称 beta-1,3-glucuronyltransferase 3 (glucuronosyltransferase I)
别名 Beta-1,3-glucuronyltransferase 3, EC:2.4.1.135, Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 3, GlcAT I, GLCATI
计算分子量 335 aa, 37 kDa
观测分子量37-40 kDa
GenBank蛋白编号BC007906
基因名称 B3GAT3
Gene ID (NCBI) 26229
RRIDAB_3741889
偶联类型 Unconjugated
形式Liquid
纯化方式Antigen affinity purification
UNIPROT IDO94766
储存缓冲液 PBS only, pH 7.3.
储存条件Store at -80°C.
The product is shipped with ice packs. Upon receipt, store it immediately at -80°C

背景介绍

B3GAT3 (Beta-1,3-Glucuronyltransferase 3), also known as Glucuronosyltransferase I (GlcAT-I), is an enzyme encoded by the B3GAT3 gene. This enzyme belongs to the glycosyltransferase family and catalyzes the transfer of glucuronic acid (GlcA) from UDP-GlcA to the terminal galactose residue of the linkage region tetrasaccharide (GlcA-Gal-Gal-Xyl-) during the biosynthesis of proteoglycans. The addition of glucuronic acid is a critical step in forming the glycosaminoglycan-protein linkage region, which serves as the attachment site for heparan sulfate and chondroitin sulfate chains. Mutations in the B3GAT3 gene cause a rare autosomal recessive disorder known as linkeropathy or B3GAT3-related multiple joint dislocations.

Loading...
||
New chat

Able

正在加载,请稍候...