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In vivo Grade Recombinant Anti

-mouse CD4 Monoclonal Antibody, Mouse IgG2a Kappa (Clone: GK1.5)
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  • ¥4000
  • Syd Labs已认证
  • 美国
  • PA007200.m2a
  • 2026年01月12日
  • ELISA, WB, Flow cytometry, IHC, ICC, animal model study
  • Mouse
  • Mouse
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 亚型

      Mouse IgG2a 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

      Mouse

    • 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。

    • 库存

      3 weeks

    • 供应商

      青木生物技术(武汉)有限公司

    • 宿主

      Mouse

    • 应用范围

      ELISA, WB, Flow cytometry, IHC, ICC, animal model study

    • 浓度

      以实际发货为准

    • 靶点

      CD4

    • 抗体英文名

      In vivo Grade Recombinant Anti-mouse CD4 Monoclonal Antibody, Mouse IgG2a Kappa (Clone: GK1.5)

    • 抗体名

      In vivo Grade Recombinant Anti-mouse CD4 Monoclonal Antibody, Mouse IgG2a Kappa (Clone: GK1.5)

    • 规格

      5mg

    The anti-mouse CD4 monoclonal antibody (clone: GK1.5) was produced in mammalian cells. The in vivo grade recombinant rat monoclonal antibody (clone: GK1.5) specifically binds to the mouse T cell receptor CD4.

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    图标文献和实验
    相关实验
    • Rapid Isotyping of Mouse Monoclonal Antibodies

      from serum, valence, and avidity, all depend on isotype. Isotyping is a basis for the selection of antibody purification, conjugation, fragmentation, and storage procedures, and predicts cytotoxic properties and half-life in vivo (see Note 1 ). In addition

    • Production of Monoclonal Antibody by DNA Immunization with Electroporation

      construct was injected intramuscularly with in vivo electroporation into mice, and the specific antibody production in mice was analyzed by enzyme-linked immunosorbent assay (ELISA). Hybridomas were generated by fusing mouse splenocytes with myeloma cells

    • 【翻译】Development trends for monoclonal antibody cancer therapeutics

      ). However, since 2000, humanized and human mAbs have been entering clinical study at approximately the same rate (4.3 versus 4.5 mAbs per year, respectively). Figure 1 | Categories of monoclonal antibody cancer therapeutics entering clinical study during 1980–1989

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