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Claudin-4 Polyclonal Antibody
Datasheet   

  • Catalog Number:

    E20-70951

  • Amount:

    100ul

  • Molecular Weight:

    22077Da

  • Applications:

    WB;IHC-p;IF(paraffin section);ELISA

  • Reactivity:

    Human;Mouse

  • Purification:

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

  • Immunogen:

    The antiserum was produced against synthesized peptide derived from human Claudin 4. AA range:160-209

  • Source:

    Polyclonal, Rabbit,IgG

  • Western Blot analysis of various cells using Claudin-4 Polyclonal Antibody diluted at 1:2000

  • Gene Name:

    CLDN4

  • Dilution:

    Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. Immunofluorescence: 1/200 - 1/1000. ELISA: 1/5000. Not yet tested in other applications.

  • Protein Name:

    Claudin-4

  • Human Gene Id:

    1364

  • Human Swiss Prot No:

    O14493

  • Mouse Gene Id:

    12740

  • Mouse Swiss Prot No:

    O35054

  • Specificity:

    Claudin-4 Polyclonal Antibody detects endogenous levels of Claudin-4 protein.

  • Formulation:

    Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

  • Concentration:

    1 mg/ml

  • Storage Stability:

    -20°C/1 year

  • Other Name:

    CLDN4; CPER; CPETR1; WBSCR8; Claudin-4; Clostridium perfringens enterotoxin receptor; CPE-R; CPE-receptor; Williams-Beuren syndrome chromosomal region 8 protein

  • Observed Band(KD):

    22

  • Background:

    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],

  • Function:

    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.,

  • Subcellular Location:

    Cell junction, tight junction . Cell membrane ; Multi-pass membrane protein . CLDN4 is required for tight junction localization in the kidney. .

  • Expression:

    Colon,Fetal brain,Trachea,Products Images

  • Western Blot analysis of HeLa cells using Claudin-4 Polyclonal Antibody diluted at 1:2000

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Catalog Number

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Claudin-4 Polyclonal Antibody | EnoGene Biotech Co. Ltd