Avelumab Biosimilar, Human PD-L1 Monoclonal Antibody

Avelumab Biosimilar, Human PD-

L1 Monoclonal Antibody
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  • ¥1000 - 9600
  • Syd Labs已认证
  • 美国
  • C023P
  • 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 PD-L1

    • 亚型

      Human IgG1

    • 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 PD-L1

    • 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

      PD-L1

    • 抗体英文名

      Avelumab Biosimilar, Human PD-L1 Monoclonal Antibody

    • 抗体名

      Avelumab Biosimilar, Human PD-L1 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 Avelumab biosimilar research grade? Avelumab is a humanized monoclonal antibody directed against the human protein ligand PD-L1 (B7-H1 or CD274, programmed cell death ligand 1), with potential antibody-dependent cell-mediated cytotoxicity property. Avelumab is used for the treatment of several kinds of carcinoma. Avelumab biosimilar uses the same protein sequences as the therapeutic antibody of Avelumab. PD-L1 (B7-H1 or CD274, programmed cell death ligand 1) and PD-L2 (B2-DC or CD273, programmed cell death ligand 2) are the two ligands for the receptor PD-1 (CD279, programmed death 1). PD-L1 is an immune checkpoint molecule expressed on both tumor cells and certain immune cells. The binding of PD-L1 to its receptors PD-1 or B7.1 on activated T cells causes an inhibitory signal to suppress their production in the lymph nodes, thereby preventing immune responses to events such as pregnancy or autoimmune disease. This pathway is also utilized by cancer cells to evade the immune system through evasion of anti-tumor T-cell response. Furthermore, over-expression of PD-L1 and PD-1 has been linked to increased tumor aggressiveness and poorer prognosis. Avelumab binds directly and selectively to PD-L1 and blocks interaction with both PD-1 and B7.1 receptors, thus reinvigorates and enhances the body’s adaptive anti-cancer activity. Disrupting the PD-L1/B7.1 interaction may also enhance T-cell priming, which could result in increased duration of response and survival.

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