GALNT17 Antibody, FITC conjugated

产品详情

产品名称：

Rabbit anti-Homo sapiens (Human) GALNT17 Polyclonal antibody
Uniprot No.：

Q6IS24
基因名：

GALNT17
别名：

GALNT17 antibody; WBSCR17Polypeptide N-acetylgalactosaminyltransferase 17 antibody; EC 2.4.1.41 antibody; Polypeptide GalNAc transferase-like protein 3 antibody; GalNAc-T-like protein 3 antibody; pp-GaNTase-like protein 3 antibody; Protein-UDP acetylgalactosaminyltransferase-like protein 3 antibody; UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase-like protein 3 antibody; Williams-Beuren syndrome chromosomal region 17 protein antibody
宿主：

Rabbit
反应种属：

Human
免疫原：

Recombinant Human Polypeptide N-acetylgalactosaminyltransferase 17 protein (101-300AA)
免疫原种属：

Homo sapiens (Human)
标记方式：

FITC
克隆类型：

Polyclonal
抗体亚型：

IgG
纯化方式：

>95%, Protein G purified
浓度：

It differs from different batches. Please contact us to confirm it.
保存缓冲液：

Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
产品提供形式：

Liquid
储存条件：

Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
货期：

Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
用途：

For Research Use Only. Not for use in diagnostic or therapeutic procedures.

功能：

May catalyze the initial reaction in O-linked oligosaccharide biosynthesis, the transfer of an N-acetyl-D-galactosamine residue to a serine or threonine residue on the protein receptor.
基因功能参考文献：
1. GWA study identified maternal genetic effects not previously identified in ASD at a locus in WBSCR17. PMID: 27876814
2. a subset of O-glycosylation produced by WBSCR17 controls dynamic membrane trafficking, probably between the cell surface and the late endosomes through macropinocytosis PMID: 22787146
相关疾病：

WBSCR17 is located in the Williams-Beuren syndrome (WBS) critical region. WBS results from a hemizygous deletion of several genes on chromosome 7q11.23, thought to arise as a consequence of unequal crossing over between highly homologous low-copy repeat sequences flanking the deleted region.
亚细胞定位：

Golgi apparatus membrane; Single-pass type II membrane protein.
蛋白家族：

Glycosyltransferase 2 family, GalNAc-T subfamily
组织特异性：

Highly expressed in brain and heart. Weakly expressed in kidney, liver, lung and spleen.
数据库链接：

HGNC: 16347

OMIM: 615137

KEGG: hsa:64409

STRING: 9606.ENSP00000329654

UniGene: Hs.488591