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IHC-P analysis of human muscle tissue using GTX47763 Claudin 11 antibody at 4.0-8.0microg/ml.
IHC-P analysis of human muscle tissue using GTX47763 Claudin 11 antibody at 4.0-8.0microg/ml.
IHC-P analysis of human muscle tissue using GTX47763 Claudin 11 antibody at 4.0-8.0microg/ml.

Claudin 11 antibody, C-term

GTX47763
GeneTex
ApplicationsImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
DownloadDatasheet
Product group Antibodies
TargetCLDN11
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Overview

  • Supplier
    GeneTex
  • Product Name
    Claudin 11 antibody, C-term
  • Delivery Days Customer
    9
  • Application Supplier Note
    IHC-P: 2-10 ug/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.5-1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID5010
  • Target name
    CLDN11
  • Target description
    claudin 11
  • Target synonyms
    claudin-11; HLD22; oligodendrocyte transmembrane protein; oligodendrocyte-specific protein; OSP; OTM
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDO75508
  • Protein Name
    Claudin-11
  • Scientific Description
    This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. The protein encoded by this gene is a major component of central nervous system (CNS) myelin and plays an important role in regulating proliferation and migration of oligodendrocytes. Mouse studies showed that the gene deficiency results in deafness and loss of the Sertoli cell epithelial phenotype in the testis. This protein is a tight junction protein at the human blood-testis barrier (BTB), and the BTB disruption is related to a dysfunction of this gene. Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Aug 2010]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

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