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Tremelimumab Biosimilar, Human

CTLA-4 monoclonal antibody
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  • ¥1000 - 9600
  • Syd Labs已认证
  • 美国
  • C037P
  • 2026年03月07日
  • Flow cytometry, animal model study
  • Mouse
  • Human
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 免疫原

      Human CTLA-4

    • 亚型

      Human IgG2

    • 形态

      Liquid

    • 保存条件

      Store at 2-8℃ and protected from prolonged exposure to light. Avoid freeze/thaw cycles.

    • 克隆性

      Monoclonal Antibody

    • 适应物种

      Human

    • 保质期

      如果保存在2 至 8°C,自收到之日起可保存1个月。如果保存在-20 至 -70°C,自收到之日起可保存 12个月。

    • 抗原来源

      Human CTLA-4

    • 库存

      1 week

    • 供应商

      青木生物技术(武汉)有限公司

    • 宿主

      Mouse

    • 应用范围

      Flow cytometry, animal model study

    • 浓度

      以实际发货为准

    • 靶点

      CTLA-4

    • 抗体英文名

      Tremelimumab Biosimilar, Human CTLA-4 monoclonal antibody

    • 抗体名

      Tremelimumab Biosimilar, Human CTLA-4 monoclonal antibody

    • 规格

      1mg/5mg/20mg

    规格:1mg产品价格:¥1000.0
    规格:5mg产品价格:¥4800.0
    规格:20mg产品价格:¥9600.0
    What is Tremelimumab biosimilar research grade? Tremelimumab (formerly ticilimumab) is a fully human monoclonal antibody against CTLA-4 / CD152. It is an immune checkpoint blocker. Unlike Ipilimumab (another fully human anti-CTLA-4 / CD152 monoclonal antibody), which is an IgG1 isotype, tremelimumab is an IgG2 isotype.Tremelimumab Biosimilar uses the same protein sequences as the therapeutic antibody tremelimumab. Tremelimumab aims to stimulate an immune system attack on tumors. Cytotoxic T lymphocytes (CTLs) can recognize and destroy cancer cells. However, there is also an inhibitory mechanism (immune checkpoint) that interrupts this destruction. Tremelimumab turns off this inhibitory mechanism and allows CTLs to continue to destroy the cancer cells. This is immune checkpoint blockade. Tremelimumab binds to the protein CTLA-4 / CD152, which is expressed on the surface of activated T lymphocytes and inhibits the killing of cancer cells. Tremelimumab blocks the binding of the antigen-presenting cell ligands B7.1 and B7.2 to CTLA-4 / CD152, resulting in inhibition of B7-CTLA-4-mediated downregulation of T-cell activation; subsequently, B7.1 or B7.2 may interact with another T-cell surface receptor protein, CD28, resulting in a B7-CD28-mediated T-cell activation unopposed by B7-CTLA-4-mediated inhibition.

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