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货号:BSCY0619

Claudin 3 Rabbit mAb

C7orf1;Claudin-3;Claudin3;CLD3_HUMAN;CLDN 3;Cldn3;Clostridium perfringens enterotoxin receptor 2;CPE R2;CPE receptor 2;CPE-R 2;CPE-receptor 2;CPETR 2;CPETR2;HRVP 1;HRVP1;Rat ventral prostate 1 like protein;Rat ventral prostate.1 protein homolog;RVP1;Ventr

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别名 C7orf1;Claudin-3;Claudin3;CLD3_HUMAN;CLDN 3;Cldn3;Clostridium perfringens enterotoxin receptor 2;CPE R2;CPE receptor 2;CPE-R 2;CPE-receptor 2;CPETR 2;CPETR2;HRVP 1;HRVP1;Rat ventral prostate 1 like protein;Rat ventral prostate.1 protein homolog;RVP1;Ventr
基因名称 Claudin 3
蛋白名称 C7orf1;Claudin-3;Claudin3;CLD3_HUMAN;CLDN 3;Cldn3;Clostridium perfringens enterotoxin receptor 2;CPE R2;CPE receptor 2;CPE-R 2;CPE-receptor 2;CPETR 2;CPETR2;HRVP 1;HRVP1;Rat ventral prostate 1 like protein;Rat ventral prostate.1 protein homolog;RVP1;Ventr
推荐应用
反应物种 Human,Mouse,Rat
存储缓冲液 PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
Human Gene Link 1365
Human Swissprot No. O15551
Mouse Gene ID 12739
Mouse Swissprot No. Q9Z0G9
Rat Gene ID 65130
Rat Swissprot No. Q63400
特异性 endogenous
稀释度 WB 1:1000-1:5000;ELISA 1:5000-1:20000;IP 1:50-1:200;
参考分子量 MW(Observed):20kD
预测分子量 MW(Calculated):23kD
运输及保存条件 -15°C to -25°C/1 year(Do not lower than -25°C)
宿主 Rabbit
同种型 IgG,Kappa
背景介绍 Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets, forming continuous seals around cells and serving as a physical barrier to prevent solutes and water from passing freely through the paracellular space. These junctions are comprised of sets of continuous networking strands in the outwardly facing cytoplasmic leaflet, with complementary grooves in the inwardly facing extracytoplasmic leaflet. The protein encoded by this intronless gene, a member of the claudin family, is an integral membrane protein and a component of tight junction strands. It is also a low-affinity receptor for Clostridium perfringens enterotoxin, and shares aa sequence similarity with a putative apoptosis-related protein found in rat. [provided by RefSeq, Jul 2008],
细胞定位 Membranous
功能 Disease:Haploinsufficiency of CLDN3 may be the cause of certain cardiovascular and musculo-skeletal abnormalities observed in Williams-Beuren syndrome (WBS), a rare developmental disorder. It is a contiguous gene deletion syndrome involving genes from chromosome band 7q11.23.,Function:Plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity.,similarity:Belongs to the claudin family.,subunit:Can form homo- and heteropolymers with other CLDN. Homopolymers interact with CLDN1 and CLDN2 homopolymers. Directly interacts with TJP1/ZO-1, TJP2/ZO-2 and TJP3/ZO-3.,
纯化 Protein A
Clonality Monoclonal
修饰类型 Unmodified
细胞定位 Membranous
组织表达 Colon/ Appendix
研究领域 >>Cell adhesion molecules;>>Tight junction;>>Leukocyte transendothelial migration;>>Pathogenic Escherichia coli infection;>>Hepatitis C

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