Cemiplimab Biosimilar, PD-1 Monoclonal Antibody

Cemiplimab Biosimilar, PD-1 Mo

noclonal Antibody
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  • ¥1000 - 9600
  • Syd Labs已认证
  • 美国
  • C029P
  • 2025年11月04日
  • Flow cytometry, animal model study
  • Mouse
  • Human
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    • 详细信息
    • 技术资料
    • 免疫原

      Human PD1

    • 亚型

      Human IgG4 kappa

    • 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 PD1

    • 库存

      4 weeks

    • 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

      PD1

    • 抗体英文名

      Cemiplimab Biosimilar, PD-1 Monoclonal Antibody

    • 抗体名

      Cemiplimab Biosimilar, PD-1 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
    Cemiplimab Biosimilar uses the same protein sequences as the therapeutic antibody cemiplimab. PD-L1 and PD-L2 (B2-DC or CD273, programmed cell death ligand 2) are the two ligands for the receptor PD-1 (CD279, programmed cell death protein 1). Cemiplimab (anti-PD-1) is an intravenous human monoclonal antibody directed against programmed cell death-1 receptor (PD-1) and blocks its interaction with programmed death ligands 1 (PD-L1) and 2 (PD-L2). Cemiplimab blocks T-cell inactivation and enhances the immune system's anti-tumor response. Binding of the programmed death receptor (PD) ligands PD-L1 and PD-L2, to the PD-1 receptor inhibits T-cell proliferation and cytokine production. The upregulation of PD-1 ligands occurs in some tumors and signaling through this pathway may contribute to the inhibition of active T-cell immune surveillance of tumors. Cemiplimab is a recombinant human immunoglobulin G4 (IgG4) monoclonal antibody that binds to the PD-1 receptor and blocks its interaction with PD-L1 and PD-L2 ligands, causing PD-1 pathway-mediated inhibition of the immune response, including the anti-tumor immune response. In mouse tumor models, blocking PD-1 activity resulted in decreased rates of tumor growth.

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