SPOP antibody

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  • 抗体类型:多克隆
  • 抗体来源:
  • 抗体应用:ELISA, WB, IP, IF
  • 特异性:Human,Mouse,Rat; other species not tested.

产品详情

  • 产品名称
    SPOP antibody
  • 抗体类型
    多克隆
  • 抗体来源
  • 抗体亚型
    兔IgG
  • 抗体描述
    SPOP Rabbit Polyclonal antibody. Positive IP detected in HeLa cells. Positive WB detected in HeLa cells, HepG2 cells, MCF-7 cells. Positive IF detected in HepG2 cells. Observed molecular weight by Western-blot: 42 kDa
  • 抗体应用
    ELISA, WB, IP, IF
  • 应用推荐

    Recommended Dilution:

    WB: 1:200-1:2000

    IP: 1:200-1:1000

    IF: 1:50-1:500

  • 特异性
    Human,Mouse,Rat; other species not tested.
  • 蛋白别名
    HIB homolog 1, Roadkill homolog 1, speckle type POZ protein, SPOP, TEF2
  • 制备方法
    This antibody was obtained by immunization of SPOP recombinant protein (Accession Number: XM_005257724). Purification method: Antigen affinity purified.
  • 组分
    PBS with 0.1% sodium azide and 50% glycerol pH 7.3.
  • 储存方法
    Store at -20℃. DO NOT ALIQUOT
  • 背景介绍
    The SPOP (TEF2) protein was previously identified as an autoantigen in a patient with scleroderma pigmentosum. SPOP (speckle-type POZ protein), also known as TEF2, HIB homolog 1 or Roadkill homolog 1, is a member of the Tdpoz family containing one N-terminal MATH (Meprin and TRAF Homology) domain and one C-terminal BTB/POZ domain. SPOP can exist as a homodimer and is expressed in a variety of tissues localizing to the nucleus. Through an interaction with CUL-3, SPOP is involved in ubiquitinylation and protein degradation. SPOP specifically interacts with CUL-3 via its BTB/POZ domain and recruits substrates to the CUL-3-based ubiquitin ligase via its MATH domain. Substrates recruited by SPOP and targeted for ubiquitylation via the CUL-3/SPOP complex include PDX-1, Bmi-1, MacroH2A, PIPK II ∫ and Daxx. These substrates are subsequently degraded by the proteasome. In addition, SPOP itself becomes ubiquitylated by the CUL-3-based ubiquitin ligase and is targeted for proteasomal degradation.
  • 参考文献
    • Gao K, Jin X, Tang Y. Tumor suppressor SPOP mediates the proteasomal degradation of progesterone receptors (PRs) in breast cancer cells. American journal of cancer research. 5(10):3210-20. 2015.
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