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B4GALT7 Polyclonal antibody

B4GALT7 Polyclonal Antibody for ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human

Applications

ELISA and More (1)

Conjugate

Unconjugated

Cat no : 10535-1-AP

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Synonyms

B4GAL T7, B4GALT7, Beta 1,4 GalTase 7, beta4Gal T7, XGALT 1, XGALT1, XGPT, XGPT1



产品信息

10535-1-AP targets B4GALT7 in WB, ELISA applications and shows reactivity with human samples.

Tested Applications ELISA Application Description
Cited ApplicationsWB
Tested Reactivity human
Cited Reactivityhuman
Immunogen B4GALT7 fusion protein Ag0793 种属同源性预测
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Full Name xylosylprotein beta 1,4-galactosyltransferase, polypeptide 7 (galactosyltransferase I)
Synonyms B4GAL T7, B4GALT7, Beta 1,4 GalTase 7, beta4Gal T7, XGALT 1, XGALT1, XGPT, XGPT1
Calculated Molecular Weight 37 kDa
Observed Molecular Weight 37 kDa
GenBank Accession NumberBC007317
Gene Symbol B4GALT7
Gene ID (NCBI) 11285
RRIDAB_2274457
Conjugate Unconjugated
Form Liquid
Purification MethodAntigen affinity purification
UNIPROT IDQ9UBV7
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

背景介绍

B4GALT7 (Beta-1,4-galactosyltransferase 7), also known as galactosyltransferase I, is involved in the formation of proteoglycans which are components of the extracellular matrix in connective tissues (PubMed: 10438455). The reduced activity of B4GALT7 results in delayed wound repair, altered migration, adhesion and contractility of patient fibroblasts (PMID: 16583246, PMID: 18158310). Mutations in B4GALT7 that also result in Spondylodysplastic (PMID: 24755949, PMID: 12417421).

实验方案

Product Specific Protocols
WB protocol for B4GALT7 antibody 10535-1-APDownload protocol
Standard Protocols
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发表文章

SpeciesApplicationTitle
humanWB

Eur J Hum Genet

Impairment of glycosaminoglycan synthesis in mucopolysaccharidosis type IIIA cells by using siRNA: a potential therapeutic approach for Sanfilippo disease.

Authors - Dziedzic Dariusz D
  • KD Validated