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Alexa Fluor® 647 Mouse Anti-Mouse IL-17A Antibody (17F3)

Interleukin-17A,IL-17,Cytotoxic T-lymphocyte-associated antigen 8 (CTLA-8),Ctla8,Il17,Il17a

价格 960.00 1-2周
货号 S0B80537
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产品规格
  • 宿主来源

    Mouse
  • 抗原名称

    IL-17A
  • 分子别名

    Interleukin-17A; IL-17; Cytotoxic T-lymphocyte-associated antigen 8 (CTLA-8); Ctla8; Il17; Il17a
  • 细胞定位

    Secreted
  • Accession

    Q62386
  • 克隆号

    17F3
  • 抗体类型

    Mouse mAb
  • 抗体同种型

    IgG1,k
  • 同型对照

    S0B5964
  • 反应种属 ?

    Ms
  • 阳性样本

    Th17 polarization C57BL/6 mouse splenocytes
  • 纯化方式

    Protein G
  • 浓度

    0.5 mg/ml
  • 标记

    Alexa Fluor® 647
  • 性状

    Liquid
  • 缓冲体系

    PBS, 1% BSA, 0.09% sodium azide

  • 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
  • IL-17A a is key cytokine produced by various immune cells such as Th17 cells. It plays a crucial role in the immune response by promoting inflammation. It can induce the expression of various pro-inflammatory molecules in different cell types, including chemokines that recruit neutrophils and other immune cells to the site of infection or injury. IL-17A is involved in the defense against certain pathogens, but its excessive production is also associated with the pathogenesis of several autoimmune and inflammatory diseases like psoriasis and rheumatoid arthritis. Targeting IL-17A has become an important therapeutic strategy in the treatment of these conditions.

  • 流式分析

    • Flow cytometric analysis of IL-17A expression in Th17 polarized C57BL/6 mouse splenocytes. Th17 polarized C57BL/6 mouse splenocytes were harvested and fixed with 4% PFA and permeabilized with Intracellular Fixation & Permeabilization Buffer Set. The cells were then stained with PE Rat anti-Mouse CD3 Antibody and either Alexa Fluor® 647 Mouse IgG1, κ Isotype Control or SDT Alexa Fluor® 647 Mouse Anti-Mouse IL-17A Antibody at 2 μl/test. Total viable cells, as determined by Fixable Viability Dye 452 (S0B88801), were used for analysis. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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