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货号: YP-rAb-17487
促销价:

产品介绍

反应种属
Human,Mouse,Rat
应用范围
WB,IHC,IF,IP,ELISA
抗体类型
单克隆抗体
基因名称(Gene Name)
CLDN3 C7orf1 CPETR2
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;Ventral prostate.1 like protein;Ventral prostate.1 protein homolog
分子量(DA)
23kD
免疫原
特异性
Endogenous
组成
PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
来源
Monoclonal, Rabbit,IgG
稀释比例
IHC 1:200-1:1000; WB 1:2000-1:10000; IF 1:200-1:1000; ELISA 1:5000-1:20000; IP 1:50-1:200; Note: For IHC, we suggest antigen retrieval with TE buffer pH 9.0
纯化工艺
Protein A
浓度
1 mg/ml
储存
-15°C to -25°C/1 year(Do not lower than -25°C)
其他名称
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 ; Ventral prostate.1 like protein ; Ventral prostate.1 protein homolog
背景
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],
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.,

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