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Recombinant Human Claudin-11 (CLDN11), Truncated

ACP06699

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP06699 Target NameCLDN11
Target SynonymsCLDN11; OSP; OTM; Claudin-11; Oligodendrocyte-specific proteinFormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Protein LengthPartial
Purity>85% (SDS-PAGE)Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDO75508
Background Information
  • Uniprot Id

    O75508

  • Target Species

    Human

  • Target Name

    CLDN11

  • Target Full Name

    Claudin-11

  • Target Function

    Plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity.

  • Target Subcellular Location

    Cell junction, tight junction. Cell membrane; Multi-pass membrane protein.

  • Target Protein Families

    Claudin family

  • Target Research Area

    Immunology

  • Target Synonyms

    CLDN11; OSP; OTM; Claudin-11; Oligodendrocyte-specific protein

  • Target Background

    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.

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