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Alexa Fluor® 647 Rat Anti-Mouse GITR Antibody (DTA-1)

Tumor necrosis factor receptor superfamily member 18,Glucocorticoid-induced TNFR-related protein,CD357,Gitr,Tnfrsf18

价格 600.00 1-2周
货号 S0B80620
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产品规格
  • 宿主来源

    Rat
  • 抗原名称

    GITR
  • 分子别名

    Tumor necrosis factor receptor superfamily member 18; Glucocorticoid-induced TNFR-related protein; CD357; Gitr; Tnfrsf18
  • 细胞定位

    Cell membrane, Secreted
  • Accession

    O35714
  • 克隆号

    DTA-1
  • 抗体类型

    Rat mAb
  • 抗体同种型

    Rat IgG2b, λ
  • 同型对照

    S0B8039
  • 反应种属 ?

    Ms
  • 阳性样本

    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

    FCM

  • 稀释度

    应用 稀释度 推荐种属
    FCM 0.25μg per million cells in 100μl volume Ms
背景介绍
  • GITR (glucocorticoid-induced TNF receptor, TNFRSF18/CD357) is a cell-surface receptor of the TNF-receptor superfamily that is constitutively expressed at high levels on regulatory T cells (Tregs) and is rapidly up-regulated on activated CD4⁺/CD8⁺ T cells and NK cells; engagement of GITR by its ligand GITRL (TNFSF18) on antigen-presenting cells delivers a costimulatory signal that activates the NF-κB pathway, enhances IL-2 and IFN-γ production, up-regulates the anti-apoptotic protein Bcl-xL, and thereby amplifies effector T-cell proliferation, cytokine secretion and cytotoxicity while transiently destabilizing FoxP3 and the suppressive function of Tregs, making GITR an attractive target for cancer immunotherapy.

  • 流式分析

    • Flow cytometric analysis of GITR expression on C57BL/6 mouse splenocytes. C57BL/6 mouse splenocytes were stained with Brilliant Violet 421™ Rat Anti-Mouse CD25 Antibody and either Alexa Fluor® 647 Rat IgG2b, λ Isotype Control (left panel) or SDT Alexa Fluor® 647 Rat Anti-Mouse GITR Antibody (right panel) at 0.5 μl/test. Total viable cells, as determined by Fixable Viability Dye 777 (S0B88805), were used for analysis. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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