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phospho-IRS1 (Ser636 + Ser639)

Rabbit pAb, BF555 conjugated(bs-3201R-BF555)-100ul
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  • ¥2980
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  • bs-3201R-BF555
  • 2025年09月30日
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      100ul

    产品编号bs-3201R-BF555
    英文名称phospho-IRS1 (Ser636 + Ser639) Rabbit pAb, BF555 conjugated
    中文名称BF555标记的磷酸化胰岛素受体底物-1抗体
    英文别名IRS1(phospho S636); p-IRS1(phospho S636); IRS1(phospho S639); p-IRS1(phospho S639); IRS-1(phospho-Ser636); IRS-1(phospho-Ser639); p-IRS1; IRS1(phospho-Ser636/639); IRS1_HUMAN; Insulin receptor substrate 1; IRS-1; IRS 1;
    产品应用Flow-Cyt=1μg /test, ICC/IF=1:100-500, IF=1:100-500

    Not yet tested in other applications.
    Optimal working dilutions must be determined by the end user.

    抗体来源Rabbit
    免疫原KLH conjugated synthesised phosphopeptide derived from human IRS1 around the phosphorylation site of Ser636/639
    亚型IgG
    纯化方法affinity purified by Protein A
    克隆类型Polyclonal
    浓度1mg/ml
    储存液0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
    研究领域

    Cancer > Signal transduction

    Cardiovascular > Atherosclerosis > Diabetes associated

    Metabolism > Types of disease > Cancer

    Metabolism > Types of disease > Diabetes

    Metabolism > Types of disease > Heart disease

    Metabolism > Types of disease > Obesity

    Neuroscience > Neurology process > Metabolism

    Signal Transduction > Adapters > Cytoplasmic

    Signal Transduction > Growth Factors/Hormones > Insulin / Insulin-like

    Tags & Cell Markers > Cell Type Markers > Tumor Associated

    亚基Interacts with UBTF and PIK3CA. Interacts (via phosphorylated YXXM motifs) with PIK3R1. Interacts with ROCK1 and FER. Interacts (via PH domain) with PHIP. Interacts with GRB2. Interacts with SOCS7. Interacts (via IRS-type PTB domain) with IGF1R and INSR (via the tyrosine-phosphorylated NPXY motif). Interacts with ALK.
    亚细胞定位IRS1 is predominantly found in the cytoplasm. Nuclear localization may occur in some cell types and under specific stimuli.
    组织特异性Isoform Long and isoform Short are predominantly expressed in tissue targets of insulin metabolic effects: liver, adipose tissue and skeletal muscle but are also expressed in the peripheral nerve, kidney, pulmonary alveoli, pancreatic acini, placenta vascular endothelium, fibroblasts, monocytes, granulocytes, erythrocytes and skin. Isoform Short is preferentially expressed in fetal cells such as fetal fibroblasts, muscle, liver and kidney. Found as a hybrid receptor with IGF1R in muscle, heart, kidney, adipose tissue, skeletal muscle, hepatoma, fibroblasts, spleen and placenta (at protein level). Overexpressed in several tumors, including breast, colon, lung, ovary, and thyroid carcinomas.
    翻译后修饰Serine phosphorylation of IRS1 is a mechanism for insulin resistance. Ser-312 phosphorylation inhibits insulin action through disruption of IRS1 interaction with the insulin receptor.
    Phosphorylation of Tyr-896 is required for GRB2-binding.
    相似性Contains 1 IRS-type PTB domain.
    _x000D_ Contains 1 PH domain.
    功能May mediate the control of various cellular processes by insulin. When phosphorylated by the insulin receptor binds specifically to various cellular proteins containing SH2 domains such as phosphatidylinositol 3-kinase p85 subunit or GRB2. Activates phosphatidylinositol 3-kinase when bound to the regulatory p85 subunit.
    保存条件Shipped at 4℃. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    注意事项This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    背景资料Insulin receptor substrates (IRS) are responsible for several insulin related activities, such as glucose homeostasis, cell growth, cell transformation, apoptosis and insulin signal transduction. Serine/threonine phosphorylation of IRS1 has been demonstrated to be a negative regulator of insulin signaling and is responsible for its degradation, although IRS1 degradation pathways are not well understood. IRS1 has also been shown to be constitutively activated in cancers such as breast cancer, Wilm's tumors, and adrenal cortical carcinomas, thus making IRS1 phosphorylation and subsequent degradation an attractive therapeutic target. To date there have been four subtypes identified: IRS1, 2, 3 and 4, with IRS1 being widely expressed.

     

    应用推荐稀释比例
    {Flow-Cyt}{1μg /test}
    {ICC/IF}{1:100-500}
    {IF}{1:100-500}

     

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