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Last updated: 2014/7/7
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CLDN4 monoclonal antibody, clone 3G97

  • Catalog # : MAB8080
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  • Specification
  • Product Description:
  • Mouse monoclonal antibody raised against synthetic peptide of CLDN4.
  • Immunogen:
  • A synthetic peptide corresponding to C-terminus of human CLDN4.
  • Host:
  • Mouse
  • Reactivity:
  • Human, Rat
  • Form:
  • Liquid
  • Isotype:
  • IgG1
  • Recommend Usage:
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (20 ug/mL)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In PBS, pH 7.4 (1% BSA, 0.1% sodium azide)
  • Storage Instruction:
  • Store at 4°C for three months. For long term storage store at -20°C.
    Aliquot to avoid repeated freezing and thawing.
  • Note:
  • This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
  • Applications
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) staining in human pancreas with CLDN4 monoclonal antibody, clone 3G97 (Cat # MAB8080).
  • Application Image
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • enlarge
  • Gene Information
  • Entrez GeneID:
  • 1364
  • Gene Name:
  • CLDN4
  • Gene Alias:
  • CPE-R,CPER,CPETR,CPETR1,WBSCR8,hCPE-R
  • Gene Description:
  • claudin 4
  • Gene Summary:
  • This gene encodes an integral membrane protein, which belongs to the claudin family. The protein is a component of tight junction strands 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
  • Other Designations:
  • Clostridium perfringens enterotoxin receptor 1,Williams-Beuren syndrome chromosomal region 8 protein
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