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B4GALT7 (基因名), Beta-1,4-galactosyltransferase 7 (蛋白名), b4gt7_human.
产品名称:

Human B4GALT7/ Beta-1,4-galactosyltransferase 7 Recombinant Protein

货号:

R2491h

商标:
EIAab®
监管等级:
别名:

Proteoglycan UDP-galactose:beta-xylose beta1, 4-galactosyltransferase I, UDP-Gal:beta-GlcNAc beta-1, 4-galactosyltransferase 7, UDP-galactose:beta-N-acetylglucosamine beta-1, 4-galactosyltransferase 7, UDP-galactose:beta-xylose beta-1, 4-galactosyltransferase, XGPT, XGalT-1, Xylosylprotein 4-beta-galactosyltransferase, Xylosylprotein beta-1, 4-galactosyltransferase, UNQ748/PRO1478, Beta-1, 4-GalTase 7, XGALT1

序列号:
Q9UBV7
来源:
E.coli
种属:
Human
标签:
His
纯度:
>90% by SDS-PAGE
浓度:
Reconstitution Dependent
形态:
Liquid
内毒素水平:
Please contact protein@eiaab.com The technician for more information.
应用:
存储缓冲液:
50mM NaH2PO4, 500mM NaCl Buffer with 500mM Imidazole, 10%glycerol(PH8.0)
存储:
Store at -20°C. (Avoid repeated freezing and thawing.)
研究领域:
Cancer
Human B4GALT7 Protein
规格 & 价格: cart
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Human B4GALT7 Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS
在线询价


R&D 技术数据
更多信息,请参阅手册,或联系我们的技术支持: tech@eiaab.com.
基因位点
Cytogenetic band: 5q35.3 by HGNC 5q35.3 by Entrez Gene 5q35.3 by Ensembl
B4GALT7 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
基因位点
通用注释


亚单元:
N/A


功能:
Required for the biosynthesis of the tetrasaccharide linkage region of proteoglycans, especially for small proteoglycans in skin fibroblasts.


亚细胞位置:
Golgi apparatus Golgi stack membrane Single-pass type II membrane protein Cis cisternae of Golgi stack.


该产品尚未在任何出版物中被引用。

[1].
"Crystal structures of β-1,4-galactosyltransferase 7 enzyme reveal conformational changes and substrate binding."

[2].
"A novel missense mutation in the galactosyltransferase-I (B4GALT7) gene in a family exhibiting facioskeletal anomalies and Ehlers-Danlos syndrome resembling the progeroid type."

[3].
"Human homolog of Caenorhabditis elegans sqv-3 gene is galactosyltransferase I involved in the biosynthesis of the glycosaminoglycan-protein linkage region of proteoglycans."

[4].
"Cloning and expression of a proteoglycan UDP-galactose:beta-xylose beta1,4-galactosyltransferase I. A seventh member of the human beta4-galactosyltransferase gene family."

[5].
"Molecular basis for the progeroid variant of Ehlers-Danlos syndrome. Identification and characterization of two mutations in galactosyltransferase I gene."

[6].
"Changes in heparan sulfate are associated with delayed wound repair, altered cell migration, adhesion and contractility in the galactosyltransferase I (beta4GalT-7) deficient form of Ehlers-Danlos syndrome."

[7].
"Defective glycosylation of decorin and biglycan, altered collagen structure, and abnormal phenotype of the skin fibroblasts of an Ehlers-Danlos syndrome patient carrying the novel Arg270Cys substitution in galactosyltransferase I (beta4GalT-7)."

[8].
"Complete sequencing and characterization of 21,243 full-length human cDNAs."

[9].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."

[10].
"The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment."
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