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FACS analysis of human peripheral blood using GTX80131 CD40 antibody [HI40a] (FITC).
FACS analysis of human peripheral blood using GTX80131 CD40 antibody [HI40a] (FITC).
FACS analysis of human peripheral blood using GTX80131 CD40 antibody [HI40a] (FITC).

CD40 antibody [HI40a] (FITC)

GTX80131
GeneTex
ApplicationsFlow Cytometry
Product group Antibodies
TargetCD40
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Overview

  • Supplier
    GeneTex
  • Product Name
    CD40 antibody [HI40a] (FITC)
  • Delivery Days Customer
    9
  • Application Supplier Note
    FACS: 20 microl reagent / 100 microl of whole blood or 106 cells in a suspension. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Flow Cytometry
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    HI40a
  • Conjugate
    FITC
  • Gene ID958
  • Target name
    CD40
  • Target description
    CD40 molecule
  • Target synonyms
    B cell surface antigen CD40; B cell-associated molecule; Bp50; CD40 molecule, TNF receptor superfamily member 5; CD40L receptor; CDW40; p50; TNFRSF5; tumor necrosis factor receptor superfamily member 5
  • Host
    Mouse
  • Isotype
    IgG1
  • Protein IDP25942
  • Protein Name
    Tumor necrosis factor receptor superfamily member 5
  • Scientific Description
    This gene is a member of the TNF-receptor superfamily. The encoded protein is a receptor on antigen-presenting cells of the immune system and is essential for mediating a broad variety of immune and inflammatory responses including T cell-dependent immunoglobulin class switching, memory B cell development, and germinal center formation. AT-hook transcription factor AKNA is reported to coordinately regulate the expression of this receptor and its ligand, which may be important for homotypic cell interactions. Adaptor protein TNFR2 interacts with this receptor and serves as a mediator of the signal transduction. The interaction of this receptor and its ligand is found to be necessary for amyloid-beta-induced microglial activation, and thus is thought to be an early event in Alzheimer disease pathogenesis. Mutations affecting this gene are the cause of autosomal recessive hyper-IgM immunodeficiency type 3 (HIGM3). Multiple alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported. [provided by RefSeq, Nov 2014]
  • Storage Instruction
    2°C to 8°C
  • UNSPSC
    12352203

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