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B3GALNT1 (基因名), UDP-GalNAc:beta-1,3-N-acetylgalactosaminyltransferase 1 (蛋白名), b3gl1_human.
产品名称:

Human B3GALNT1/ UDP-GalNAc:beta-1,3-N-acetylgalactosaminyltransferase 1 Recombinant Protein
UDP-GalNAc: beta 1, 3-N-acetylgalactosaminyltransferase 1

货号:

R2486h

商标:
EIAab®
监管等级:
别名:

Beta-1, 3-galactosyltransferase 3, Beta-3-Gx-T3, Galactosylgalactosylglucosylceramide beta-D-acetyl-galactosaminyltransferase, Globoside synthase, UDP-N-acetylgalactosamine:globotriaosylceramide beta-1, 3-N-acetylgalactosaminyltransferase, Beta-1, 3-GalTase 3, UNQ531/PRO1074, Beta-1, 3-GalNAc-T1, B3GALT3

序列号:
O75752
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:
-
Human B3GALNT1 Protein
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Human B3GALNT1 Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS
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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: 3q26.1 by HGNC 3q26.1 by Entrez Gene 3q26.1 by Ensembl
B3GALNT1 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:
Transfers N-acetylgalactosamine onto globotriaosylceramide.


亚细胞位置:
Golgi apparatus membrane Single-pass type II membrane protein


该产品尚未在任何出版物中被引用。

[1].
"Expression cloning of human globoside synthase cDNAs. Identification of beta 3Gal-T3 as UDP-N-acetylgalactosamine:globotriaosylceramide beta 1,3-N-acetylgalactosaminyltransferase."

[2].
"A family of human beta3-galactosyltransferases. Characterization of four members of a UDP-galactose:beta-N-acetyl-glucosamine/beta-nacetyl-galactosamine beta-1,3-galactosyltransferase family."

[3].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."

[4].
"The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment."

[5].
"Molecular basis of the globoside-deficient P(k) blood group phenotype. Identification of four inactivating mutations in the UDP-N-acetylgalactosamine: globotriaosylceramide 3-beta-N-acetylgalactosaminyltransferase gene."

[6].
"Architecture of the human interactome defines protein communities and disease networks."

[7].
"Identification of the Molecular and Genetic Basis of PX2, a Glycosphingolipid Blood Group Antigen Lacking on Globoside-deficient Erythrocytes."

[8].
"The BioPlex Network: A Systematic Exploration of the Human Interactome."

[9].
"[A rare Pk phenotype caused by a 433 C>T mutation of the β-1,3-N-acetylgalactosyltransferase gene]."

[10].
"α-1,3-N-acetylgalactose aminotransferase gene 539G>C mutation leads to the A2B isoform."
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