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InVivoMAb anti-mouse 4-1BB (CD137)

Research Use Only
BE0169
Bio X Cell
ApplicationsOther Application
Product group Antibodies
ReactivityMouse
Price on request
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Overview

  • Supplier
    Bio X Cell
  • Product Name
    InVivoMAb anti-mouse 4-1BB (CD137)
  • Delivery Days Customer
    7
  • Applications
    Other Application
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    LOB12.3
  • Concentration
    4-11 mg/ml
  • Host
    Rat
  • Isotype
    IgG1
  • Reactivity
    Mouse
  • Storage Instruction
    2°C to 8°C
  • UNSPSC
    12352203

References

  • Optimization of 4-1BB antibody for cancer immunotherapy by balancing agonistic strength with FcgammaR affinity. Qi X et al., 2019 May 20, Nat Commun
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  • Unique potential of 4-1BB agonist antibody to promote durable regression of HPV+ tumors when combined with an E6/E7 peptide vaccine. Bartkowiak T et al., 2015 Sep 22, Proc Natl Acad Sci U S A
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  • Curing mice with large tumors by locally delivering combinations of immunomodulatory antibodies. Dai M et al., 2015 Mar 1, Clin Cancer Res
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  • Anaphylaxis caused by repetitive doses of a GITR agonist monoclonal antibody in mice. Murphy JT et al., 2014 Apr 3, Blood
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  • Combinatorial PD-1 blockade and CD137 activation has therapeutic efficacy in murine cancer models and synergizes with cisplatin. Wei H et al., 2013, PLoS One
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  • Combined TIM-3 blockade and CD137 activation affords the long-term protection in a murine model of ovarian cancer. Guo Z et al., 2013 Sep 17, J Transl Med
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  • Long-lasting complete regression of established mouse tumors by counteracting Th2 inflammation. Dai M et al., 2013 May, J Immunother
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  • CD4+ T cells develop antiretroviral cytotoxic activity in the absence of regulatory T cells and CD8+ T cells. Manzke N et al., 2013 Jun, J Virol
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  • Localized immunotherapy via liposome-anchored Anti-CD137 + IL-2 prevents lethal toxicity and elicits local and systemic antitumor immunity. Kwong B et al., 2013 Mar 1, Cancer Res
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  • Combination CTLA-4 blockade and 4-1BB activation enhances tumor rejection by increasing T-cell infiltration, proliferation, and cytokine production. Curran MA et al., 2011 Apr 29, PLoS One
    Read more

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