IL-4 Antibody, anti-human, PE-Vio® 615, 100 tests in 1 mL

IL-4 Antibody, anti-human, PE-

Vio® 615, 100 tests in 1 mL
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  • 询价
  • Miltenyi Biotec已认证
  • 德国
  • 130-107-144
  • 2025年12月09日
  • Intracellular flow cytometry, Mass cytometry, Functional assay
  • mouse
  • human, non-human primate
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13钻石会员
  • 企业认证

    • 详细信息
    • 技术资料
    • 免疫原

      IL-4

    • 亚型

      mouse IgG1κ

    • 形态

      Reagents are supplied in buffer containing stabilizer and 0.05% sodium azide.

    • 保存条件

      避光,2-8℃

    • 克隆性

      7A3-3

    • 标记物

      PE-Vio 615

    • 适应物种

      human, non-human primate

    • 保质期

      24个月

    • 供应商

      Miltenyi Biotec

    • 宿主

      mouse

    • 应用范围

      Intracellular flow cytometry, Mass cytometry, Functional assay

    • 浓度

      1:10

    • 靶点

      IL-4

    • 抗体英文名

      IL-4 Antibody, anti-human

    • 抗体名

      IL-4 Antibody, anti-human

    • 规格

      100 tests in 1 mL

    Intracellular staining of IL-4–producing human or non-human primate cellsInterleukin-4 (IL-4) is predominantly secreted by activated CD4+ memory and effector Tʜ2 cells, basophils, and mast cells. It induces and supports humoral immune responses for the neutralization of extracellular pathogens. The Tʜ2 types of immune mechanisms can also be involved in immunological disorders such as IgE-mediated allergy. | The Anti-IL‑4 antibody has been designed for intracellular staining of IL‑4–producing cells. Cells can be stimulated for IL‑4–production, e.g., by polyclonal stimulation with mitogens. For induction of IL‑4 production by antigen-specific T cells, cells are restimulated with respective antigen. IL‑4 can be accumulated in the cells by addition of secretion inhibitors like brefeldin A. After fixation and permeabilization of the cell sample, IL‑4–producing cells can be stained intracellularly with the Anti-IL‑4 antibody. Staining of surface markers allows simultaneous flow cytometric analysis of subsets and activation status of the IL‑4–producing cells. Magnetically enriched cells can be stained intracellularly for IL‑4 production directly on the MACS® Column. This procedure ensures higher sensitivity of detection and minimizes loss of cells during washing procedures for cytokine analysis of rare cells, e.g., CD4+ T cells in HIV patients, or other cell sources than peripheral blood mononuclear cells (PBMCs), e.g., bronchoalveolar lavages, or synovial fluids.

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