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Rabbit Anti-CSGLCAT/AF594 Conjugated antibody (bs-20304R-AF594) ~~~促销,代码KX240301~~~
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说 明 书: 100ul  
100ul/2980.00元
大包装/询价
产品编号 bs-20304R-AF594
英文名称 Anti-CSGLCAT/AF594
中文名称 AF594标记的硫酸软骨素聚合酶3抗体
别    名 Chondroitin sulfate glucuronyltransferase; Chondroitin synthase 3; CSGlcA-T; ChSy 3; ChSy-3; CHPF2; ChPF-2; CSGLCA T; N acetylgalactosaminyl proteoglycan 3 beta glucuronosyltransferase; CHPF2_HUMAN; Chondroitin polymerizing factor 2; Chondroitin sulfate glucuronyltransferase; N acetylgalactosaminyl proteoglycan 3 beta glucuronosyltransferase; N-acetylgalactosaminyl-proteoglycan 3-beta-glucuronosyltransferase.  
规格价格 100ul/2980元 购买        大包装/询价
说 明 书 100ul  
研究领域 细胞生物  糖蛋白  细胞类型标志物  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应
产品应用 ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 86kDa
性    状 Lyophilized or Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human CSGLCAT
亚    型 IgG
纯化方法 affinity purified by Protein A
储 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
产品介绍 background:
CSGlcA-T is a 772 amino acid single-pass type II membrane protein of the golgi apparatus that belongs to the chondroitin N-acetylgalactosaminyltransferase family. Widely expressed and existing as two alternatively spliced isoforms, CSGlcA-T is found at highest levels in small intestine, pancreas and placenta, with lower levels in heart, brain, kidney, and skeletal muscle where it transfers glucuronic acid from UDP-glucuronic acid to N-acetylgalactosamine residues of elongating chondroitin polymers. The gene encoding CSGlcA-T maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome and Lissencephaly.

Function:
Transfers glucuronic acid (GlcUA) from UDP-GlcUA to N-acetylgalactosamine residues on the non-reducing end of the elongating chondroitin polymer. Has no N-acetylgalactosaminyltransferase activity.

Subcellular Location:
Golgi apparatus, Golgi stack membrane; Single-pass type II membrane protein (Probable).

Tissue Specificity:
Ubiquitous. Highly expressed in placenta, small intestine and pancreas.

Similarity:
Belongs to the chondroitin N-acetylgalactosaminyltransferase family

Database links:

Entrez Gene: 54480 Human

Entrez Gene: 100910 Mouse

Entrez Gene: 296733 Rat

Omim: 608037 Human

SwissProt: Q9P2E5 Human

Unigene: 647084 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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