SH3BP2 Rabbit pAb, APC-Cy7 conjugated(bs-19749R-APC-Cy7)-100ul

SH3BP2 Rabbit pAb, APC-Cy7 con

jugated(bs-19749R-APC-Cy7)-100ul
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  • ¥2980
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  • bs-19749R-APC-Cy7
  • 2025年09月30日
  • 产品信息以Bioss网站为准
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    • 规格

      100ul

    产品编号bs-19749R-APC-Cy7
    英文名称SH3BP2 Rabbit pAb, APC-Cy7 conjugated
    中文名称APC-Cy7标记的SH3结构域结合蛋白2抗体
    英文别名3BP-2; 3BP2; 3BP2_HUMAN; Abl SH3 binding protein 2; Cherubism; CRBM; CRPM; FLJ42079; FLJ54978; RES4-23; SH3 domain binding protein 2; SH3 domain-binding protein 2; Sh3bp2; TNFAIP3 interacting protein 2.
    产品应用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 synthetic peptide derived from human SH3BP2
    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

    Signal Transduction > Adapters > Cytoplasmic

    Signal Transduction > Signaling Pathway > Lipid Signaling

    组织特异性Expressed in a variety of tissues including lung, liver, skeletal muscle, kidney and pancreas.
    翻译后修饰Phosphorylated. Phosphorylation at Tyr-448 may stimulate the activity of the LYN kinase (By similarity).
    相似性Contains 1 PH domain.
    _x000D_ Contains 1 SH2 domain.
    功能Binds differentially to the SH3 domains of certain proteins of signal transduction pathways. Binds to phosphatidylinositols; linking the hemopoietic tyrosine kinase fes to the cytoplasmic membrane in a phosphorylation dependent mechanism.
    保存条件Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    背景资料The protein encoded by this gene has an N-terminal pleckstrin homology (PH) domain, an SH3-binding proline-rich region, and a C-terminal SH2 domain. The protein binds to the SH3 domains of several proteins including the ABL1 and SYK protein tyrosine kinases , and functions as a cytoplasmic adaptor protein to positively regulate transcriptional activity in T, natural killer (NK), and basophilic cells. Mutations in this gene result in cherubism. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]

     

    应用推荐稀释比例
    {IF}{1:100-500}

     

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