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InVivoMAb anti-mouse TIM-3 (CD366)

Research Use Only
BE0275
Bio X Cell
ApplicationsFlow Cytometry, Neutralisation/Blocking
Product group Antibodies
ReactivityMouse
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Overview

  • Supplier
    Bio X Cell
  • Product Name
    InVivoMAb anti-mouse TIM-3 (CD366)
  • Delivery Days Customer
    7
  • Applications
    Flow Cytometry, Neutralisation/Blocking
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    B8.2C12
  • Concentration
    4-11 mg/ml
  • Estimated Purity
    >95%
  • Host
    Rat
  • Isotype
    IgG1
  • Scientific Description
    The B8.2C12 monoclonal antibody reacts with mouse TIM-3 (T cell immunoglobulin and mucin domain-3) also known as CD366. This antibody binds to the BALB/c allele of TIM-3 while reactivity to the C57Bl/6 allele is significantly weaker. TIM-3 is a 60 kDa member of the TIM family of immune checkpoint receptors and exists as a type I transmembrane glycoprotein with a mucin-like domain in its extracellular portion and a tyrosine phosphorylation motif in its cytoplasmic portion. TIM-3 is specifically expressed at high levels on the surface of Th1 lymphocytes whereas Th2 lymphocytes express TIM-1 and TIM-2. TIM-3 activation occurs via binding to the cell-associated C-type lectin galectin-9. Upon binding TIM-3 induces apoptosis of Th1 cells. Inhibition of TIM-3 signaling in mice has been shown to exacerbate experimental autoimmune encephalomyelitis, promote IFNγ production and Th1 cell proliferation. Tim-3 has also been shown to be required for the induction of tolerance, as both TIM-3 knockout animals and mice treated with TIM-3-Ig fusion protein display defects in the induction of antigen-specific tolerance. Additionally, TIM-3 signaling is currently being explored as a cancer immunotherapy target as CD8 T cells which express both TIM-3 and PD-1 exhibit greater defects in both cell-cycle progression and effector cytokine production than cells that express PD-1 alone.
  • Reactivity
    Mouse
  • Storage Instruction
    2°C to 8°C
  • UNSPSC
    12352203

References

  • STT3-dependent PD-L1 accumulation on cancer stem cells promotes immune evasion. Hsu JM et al., 2018 May 15, Nat Commun
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  • Microglia activity modulated by T cell Ig and mucin domain protein 3 (Tim-3). Wang HW et al., 2015 Jan, Cell Immunol
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  • Tim-3 negatively mediates natural killer cell function in LPS-induced endotoxic shock. Hou H et al., 2014, PLoS One
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  • Requirement for interactions of natural killer T cells and myeloid-derived suppressor cells for transplantation tolerance. Hongo D et al., 2014 Nov, Am J Transplant
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  • TIM-3 regulates innate immune cells to induce fetomaternal tolerance. Chabtini L et al., 2013 Jan 1, J Immunol
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  • Interactions between NKT cells and Tregs are required for tolerance to combined bone marrow and organ transplants. Hongo D et al., 2012 Feb 9, Blood
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  • Tim-3-Galectin-9 pathway involves the suppression induced by CD4+CD25+ regulatory T cells. Wang F et al., 2009, Immunobiology
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  • TIM-1 and TIM-3 enhancement of Th2 cytokine production by mast cells. Nakae S et al., 2007 Oct 1, Blood
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  • Cutting edge: T cell Ig mucin-3 reduces inflammatory heart disease by increasing CTLA-4 during innate immunity. Frisancho-Kiss S et al., 2006 Jun 1, J Immunol
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  • Th1-specific cell surface protein Tim-3 regulates macrophage activation and severity of an autoimmune disease. Monney L et al., 2002 Jan 31, Nature
    Read more

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