Claudin-4 Polyclonal Antibody

    • 货号:YT0950
    • 应用:WB;IHC;IF;ELISA
    • 种属:Human;Rat;Mouse;
      • 靶点:
      • Claudin-4
      • 简介:
      • >>Cell adhesion molecules;>>Tight junction;>>Leukocyte transendothelial migration;>>Pathogenic Escherichia coli infection;>>Hepatitis C
      • 基因名称:
      • CLDN4
      • 蛋白名称:
      • Claudin-4
      • Human Gene Id:
      • 1364
      • Human Swiss Prot No:
      • O14493
      • Mouse Swiss Prot No:
      • O35054
      • 免疫原:
      • The antiserum was produced against synthesized peptide derived from human Claudin 4. AA range:160-209
      • 特异性:
      • Claudin-4 Polyclonal Antibody detects endogenous levels of Claudin-4 protein.
      • 组成:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • 来源:
      • Polyclonal, Rabbit,IgG
      • 稀释:
      • WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:5000.. IF 1:50-200
      • 纯化工艺:
      • The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
      • 浓度:
      • 1 mg/ml
      • 储存:
      • -15°C to -25°C/1 year(Do not lower than -25°C)
      • 其他名称:
      • CLDN4;CPER;CPETR1;WBSCR8;Claudin-4;Clostridium perfringens enterotoxin receptor;CPE-R;CPE-receptor;Williams-Beuren syndrome chromosomal region 8 protein
      • 实测条带:
      • 28kD
      • 背景:
      • The protein encoded by this intronless gene belongs to the claudin family. Claudins are integral membrane proteins that are components of the epithelial cell tight junctions, which regulate movement of solutes and ions through the paracellular space. This protein is a high-affinity receptor for Clostridium perfringens enterotoxin (CPE) and may play a role in internal organ development and function during pre- and postnatal life. This gene is deleted in Williams-Beuren syndrome, a neurodevelopmental disorder affecting multiple systems. [provided by RefSeq, Sep 2013],
      • 功能:
      • disease:Haploinsufficiency of CLDN4 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.,similarity:Belongs to the claudin family.,subunit:Directly interacts with TJP1/ZO-1, TJP2/ZO-2 and TJP3/ZO-3.,
      • 细胞定位:
      • Cell junction, tight junction . Cell membrane ; Multi-pass membrane protein . CLDN4 is required for tight junction localization in the kidney. .
      • 组织表达:
      • Colon,Fetal brain,Trachea,
      • 产品图片
      • Western Blot analysis of mouse-BRAIN cells using Claudin-4 Polyclonal Antibody diluted at 1:500
      • Immunohistochemistry analysis of paraffin-embedded human brain tissue, using Claudin 4 Antibody. The picture on the right is blocked with the synthesized peptide.
      • Western blot analysis of lysates from COLO cells, using Claudin 4 Antibody. The lane on the right is blocked with the synthesized peptide.