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Mouse Anti-Human Stat4 (pY693) Antibody (S-3782)

Signal transducer and activator of transcription 4,STAT4

价格 260.00 1-2周
货号 S0B80128
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产品介绍 评论(0)

产品规格
  • 宿主来源

    Mouse
  • 抗原名称

    Stat4 (pY693)
  • 分子别名

    Signal transducer and activator of transcription 4; STAT4
  • 细胞定位

    Nucleus
  • Accession

    Q14765
  • 克隆号

    S-3782
  • 抗体类型

    Mouse mAb
  • 抗体同种型

    IgG2b,k
  • 反应种属 ?

    Hu
  • 阳性样本

    Human PBMC
  • 纯化方式

    Protein A
  • 浓度

    2 mg/ml
  • 标记

    Unconjugated
  • 性状

    Liquid
  • 缓冲体系

    PBS pH7.4

  • 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 1:400 Hu
背景介绍
  • Stat4 (pY693) refers to the activated form of the Signal Transducer and Activator of Transcription 4 protein, specifically characterized by the phosphorylation of tyrosine residue 693, a critical post-translational modification that serves as a molecular switch for its function in immune signaling pathways. Upon stimulation by cytokines such as interleukin-12 (IL-12) and interleukin-23 (IL-23), the associated Janus kinases (JAKs) phosphorylate Stat4 at this specific tyrosine site, which induces conformational changes allowing Stat4 to dimerize via reciprocal SH2 domain-phosphotyrosine interactions. These stable dimers then translocate into the nucleus, where they bind to specific DNA response elements to regulate the transcription of target genes, most notably driving the differentiation of naive CD4+ T cells into Th1 cells and promoting the production of interferon-gamma (IFN-γ), thereby playing a pivotal role in cell-mediated immunity and inflammatory responses. Consequently, the detection of Stat4 phosphorylated at Y693 is widely used as a definitive biomarker for active IL-12/IL-23 pathway signaling in immunological research and clinical diagnostics related to autoimmune diseases.

  • 流式分析

    • Flow cytometric analysis of untreated human PBMC (human peripheral blood mononuclear cells, left) /human PBMC treated with 100ng/ml IL-2 for 30 min and 100ng/ml IFN-α2 for 30 min, right. Cells were fixed with 4% paraformaldehyde and permeabilized with 90% methanol and labeled with Human Stat4 antibody at 1/400 dilution (0.5 μg) / (red) compared with a Mouse IgG2b, κ (black) Isotype Control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (blue). Goat Anti-Mouse IgG Alexa Fluor® 488 was used as the secondary antibody. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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