GALNT17 Antibody
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货号:CSB-PA743592LA01HU
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规格:¥440
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促销:
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图片:
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其他:
产品详情
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产品名称:Rabbit anti-Homo sapiens (Human) GALNT17 Polyclonal antibody
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Uniprot No.:Q6IS24
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基因名:GALNT17
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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
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宿主:Rabbit
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反应种属:Human
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免疫原:Recombinant Human Polypeptide N-acetylgalactosaminyltransferase 17 protein (101-300AA)
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免疫原种属:Homo sapiens (Human)
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标记方式:Non-conjugated
本页面中的产品,GALNT17 Antibody (CSB-PA743592LA01HU),的标记方式是Non-conjugated。对于GALNT17 Antibody,我们还提供其他标记。见下表:
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克隆类型:Polyclonal
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抗体亚型:IgG
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纯化方式:>95%, Protein G purified
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浓度:It differs from different batches. Please contact us to confirm it.
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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
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应用范围:ELISA, IHC
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推荐稀释比:
Application Recommended Dilution IHC 1:20-1:200 -
Protocols:
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储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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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.
相关产品
靶点详情
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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.
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基因功能参考文献:
- GWA study identified maternal genetic effects not previously identified in ASD at a locus in WBSCR17. PMID: 27876814
- 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
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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.
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亚细胞定位:Golgi apparatus membrane; Single-pass type II membrane protein.
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蛋白家族:Glycosyltransferase 2 family, GalNAc-T subfamily
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组织特异性:Highly expressed in brain and heart. Weakly expressed in kidney, liver, lung and spleen.
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数据库链接:
HGNC: 16347
OMIM: 615137
KEGG: hsa:64409
STRING: 9606.ENSP00000329654
UniGene: Hs.488591
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