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TLE1/2/3/4 Antibody

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年10月27日
  • W, IF-IC
  • Rabbit
  • H,M,Mk,Dm,R,X,Z
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      TLE1/2/3/4 Antibody

    • 抗原

      synthetic peptide corresponding to residues surrounding Asp760 of human TLE1

    • 应用范围

      W, IF-IC

    • 宿主

      Rabbit

    • 库存

      大量

    • 保质期

      详见说明书

    • 适应物种

      H,M,Mk,Dm,R,X,Z

    • 级别

      详见MSDS文件

    • 供应商

      CST

    • 是否单克隆

      2

    • 保存条件

      -20°c

    • 规格

      100 ul (10 western blots)/carrier free & custom formulation / quantity

    规格:产品价格:¥请询价
    规格:100 ul (10 western blots)产品价格:¥请询价
    规格:carrier free & custom formulation / quantity产品价格:¥请询价

    pathway more info application references datasheet PDF MSDS PDF protocols

    Applications Key:  W=Western Blotting  IF-IC=Immunofluorescence (Immunocytochemistry)
    Reactivity Key:  H=Human  M=Mouse  R=Rat  Mk=Monkey  Dm=D. melanogaster  X=Xenopus  Z=Zebrafish
    Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

    Applications Reactivity Sensitivity MW (kDa) Source
    W IF-IC H M Mk Dm (R) (X) (Z) Endogenous 78-90 Rabbit
    Protocols
    Specificity / Sensitivity

    TLE1/2/3/4 Antibody detects endogenous levels of TLE1, TLE2, TLE3, and TLE4 proteins. Based on homology it should also recognize TLE1 and TLE2 of Zebra fish, TLE2 of Xenopus, and Groucho of Drosophila.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Asp760 of human TLE1. Antibodies are purified by peptide affinity chromatography.

    Western Blotting

    Western Blotting

    Western blot analysis of cell extracts from various cell types using TLE1/2/3/4 Antibody.

    IF-IC

    IF-IC

    Confocal immunofluorescent analysis of SH-SY5Y cells using TLE1/2/3/4 Antibody (green). Actin filaments have been labeled with Alexa Fluor® 555 phalloidin (red). Blue pseudocolor = DRAQ® #4084 (fluorescent DNA dye).

    Background

    Transducin-like enhancer of split proteins (TLE1, TLE2, TLE3, TLE4, and TLE6) are mammalian homologs of Drosophila Groucho (1). TLEs contain several WD-repeats implicated in protein-protein interaction (2,3). TLEs are transcriptional co-repressors that bind to many transcription factors such as LEF1, Runx1, Oct-1, hepatocyte nuclear factor 3-β as well as histone H3 (4-7). TLEs are differentially expressed during animal development and may have overlapping as well as distinct functions (8).

    1. Stifani, S. et al. (1992) Nat. Genet. 2, 119-127.
    2. Chen, G. and Courey, A.J. (2000) Gene 249, 1-16.
    3. Jennings, B.H. et al. (2006) Mol. Cell 22, 645-655.
    4. Levanon, D. et al. (1998) Proc. Natl. Acad. Sci. U S A 95, 11590-11595.
    5. Malin, S. et al. (2005) Nucleic Acids Res. 33, 4618-4625.
    6. Wang, J.C. et al. (2000) J. Biol. Chem. 275, 18418-18423.
    7. Palaparti, A. et al. (1997) J. Biol. Chem. 272, 26604-26610.
    8. Gasperowicz, M. and Otto, F. (2005) J. Cell Biochem. 95, 670-687.
    Application References

    Have you published research involving the use of our products? If so we'd love to hear about it. Please let us know !

    Companion Products

    For Research Use Only. Not For Use In Diagnostic Procedures.

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    图标文献和实验
    相关实验
    • Generation of Antibody Molecules Through Antibody Engineering

      been overcome to a large extent using genetic-engineering techniques to produce chimeric mouse/human and completely human antibodies. Such an approach is particularly suitable because of the domain structure of the antibody molecule ( 2 ), where functional

    • 【求助】关于gsk3-beta功能的疑问

      a look from the following website just by clicking "Tyrosine Phosphorylation and Dimerization" http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6WSN-43F85YV-2&_user=1111158&_coverDate=06%2F29%2F2001&_rdoc=1&_fmt=full&_orig=search

    • 新型光机结合的二维共焦生物芯片扫描仪设计

      扫描仪中,都采用机械式的二维X,Y线性扫描技术实现,即X,Y方向都采用直线驱动器和直线导轨实现往复运动。此类装置,由于驱动系统的频率限制,驱动器的扫描惯性大,使得扫描效率低,分析时间相当长;并且往复行程长,对直线导轨的精度要求相当高。二、光机结合的二维扫描系统为同样实现生物芯片的二维扫描,我们的实验装置设计如图2,采用了振镜和大数值孔径的远心f-è物镜相结合实现X方向扫描,Y方向的运动仍采用直线驱动器和直线导轨实现。 系统中,对于f-è物镜,满足x2fè(è为振镜的摆动角度,f为物镜焦距)的线性

    图标技术资料

    暂无技术资料 索取技术资料

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