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Alexa Fluor® 488 Rat Anti-Mouse IL-2 Antibody (JES6-5H4)

Interleukin-2,T-cell growth factor (TCGF),Il-2,Il2

价格 400.00 供应商现货 : 3-5个工作日
货号 S0B80352
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产品规格
  • 宿主来源

    Rat
  • 抗原名称

    IL-2
  • 分子别名

    Interleukin-2; T-cell growth factor (TCGF); Il-2; Il2
  • 细胞定位

    Secreted
  • Accession

    P04351
  • 克隆号

    JES6-5H4
  • 抗体类型

    Rat mAb
  • 抗体同种型

    IgG2b,k
  • 同型对照

    S0B5536
  • 反应种属 ?

    Ms
  • 阳性样本

    C57BL/6 mouse splenocytes stimulated for 6h with the cell stimulation cocktail
  • 纯化方式

    Protein G
  • 浓度

    0.5 mg/ml
  • 标记

    Alexa Fluor® 488
  • 性状

    Liquid
  • 缓冲体系

    PBS, 1% BSA, 0.3% Proclin 300

  • 储存条件

    12 months from date of receipt / reconstitution, 2 to 8 °C as supplied

  • 应用

    ICFCM

  • 稀释度

    应用 稀释度 推荐种属
    ICFCM 1μg per million cells in 100μl volume Ms
背景介绍
  • Interleukin-2 (IL-2) is a cytokine that plays a crucial role in the immune system. It is primarily produced by activated T cells and has multiple functions. IL-2 promotes the proliferation and differentiation of T cells, enhancing their ability to fight infections and tumors. It also stimulates the growth and activity of natural killer (NK) cells, which are important for immune defense. Additionally, IL-2 can regulate the activity of regulatory T cells (Tregs), helping to maintain immune tolerance and prevent autoimmune diseases. In clinical settings, IL-2 has been used to treat certain cancers by boosting the immune response, although its use is limited due to potential side effects. Its discovery and research have significantly advanced our understanding of the immune system and provided new strategies for immunotherapy.

  • 流式分析

    • Flow cytometric analysis of 4% PFA fixed 0.1% Tween-20 permeabilized C57BL/6 mouse splenocytes, Stimulated 6 hours with Stimulation Cocktail labelled with Alexa Fluor® 488 Rat IgG2b, k Isotype Control (left panel) or SDT Alexa Fluor® 488 Rat Anti-Mouse IL-2 Antibody at 2 μl/test (right panel). Total viable cells, as determined by Fixable Viability Dye 452 (S0D0021), were used for analysis. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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