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Alexa Fluor® 488 Armenian Hamster Anti-Mouse/Human Helios Antibody (22F6)

Zinc finger protein Helios,HELIOS,ZNFN1A2,IKZF2

价格 1,590.00 1-2周
货号 S0B80505
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产品介绍 评论(0)

产品规格
  • 宿主来源

    Armenian hamster
  • 抗原名称

    Helios
  • 分子别名

    Zinc finger protein Helios; HELIOS; ZNFN1A2; IKZF2
  • 细胞定位

    Nucleus
  • Accession

    Q9UKS7, P81183
  • 克隆号

    22F6
  • 抗体类型

    Recombinant mAb
  • 抗体同种型

    IgG
  • 反应种属 ?

    Hu, 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® 488
  • 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 0.25μg per million cells in 100μl volume Hu, Ms
背景介绍
  • Helios (encoded by the IKZF2 gene) is a member of the Ikaros family of transcription factors and contains multiple zinc finger domains that facilitate DNA binding and the formation of homodimers or heterodimers. It is predominantly expressed in T cells, regulatory T cells (Tregs), certain B cell subsets, and hematopoietic and epithelial tissues. Helios plays a crucial role in T cell activation, proliferation, and the stability and function of Tregs. Additionally, Helios has been identified as a potential biomarker in autoimmune diseases and may influence tumor development by regulating gene expression and modulating cell differentiation and proliferation.

  • 流式分析

    • C57BL/6 mouse splenocytes were stained with Alexa Fluor® 647 Mouse Anti-Human CD4 Antibody and fixed and permeabilized with the eBioscience™ Foxp3 / Transcription Factor Fixation/Permeabilization Concentrate and Diluent. The cells were then stained with either Alexa Fluor® 488 Armenian hamster IgG Isotype Control (left panel) or SDT Alexa Fluor® 488 Armenian hamster Anti-Mouse/Human Helios Antibody (right panel) at 0.5 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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