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EAPP (1E4) Mouse mAb

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2026年01月07日
  • W, IF-IC
  • H,M,R,Mk
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      EAPP (1E4) Mouse mAb

    • 抗原

      recombinant amino-terminal fragment of human EAPP protein

    • 应用范围

      W, IF-IC

    • 保质期

      详见说明书

    • 级别

      详见MSDS文件

    • 库存

      大量

    • 供应商

      CST

    • 适应物种

      H,M,R,Mk

    • 是否单克隆

      1

    • 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
    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) Isotype
    W IF-IC H M R Mk Endogenous 45 Mouse IgG1
    Protocols
    Specificity / Sensitivity

    EAPP (1E4) Mouse mAb detects endogenous levels of total EAPP protein.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a recombinant amino-terminal fragment of human EAPP protein.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from various cell types using EAPP (1E4) Mouse mAb.

    IF-IC

    IF-IC

    Confocal immunofluorescent analysis of MCF7 cells using EAPP (1E4) Mouse mAb (green). Actin filaments have been labeled with DY-554 phalloidin (red). Blue pseudocolor = DRAQ5® #4084 (fluorescent DNA dye).

    Background

    Regulation of the E2F family of transcription factors, primarily through the retinoblastoma protein (pRb), is vital for control of cell proliferation and cell death (reviewed in 1). E2F-associated phosphoprotein (EAPP) was identified as an E2F-family binding protein that modulates E2F-regulated transcription and may be required for S phase entry. EAPP is expressed at varied levels in all tissues and cell types examined and its expression is reduced in nocodazole-arrested cells (2). Mass spectrometry studies have identified multiple EAPP phosphorylation sites including Ser109 and Ser111, but biological consequences of EAPP phosphorylation have yet to be elucidated (3-5).

    1. Polager, S. and Ginsberg, D. (2008) Trends Cell Biol 18, 528-35.
    2. Novy, M. et al. (2005) Mol Biol Cell 16, 2181-90.
    3. Dephoure, N. et al. (2008) Proc Natl Acad Sci U S A 105, 10762-7.
    4. Mayya, V. et al. (2009) Sci Signal 2, ra46.
    5. Olsen, J.V. et al. (2006) Cell 127, 635-48.
    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
    • Purification of mAb (IgG)

      (adjust pH to 7.8 with Binding buffer; red color) to the Protein A column.Mouse antibodies of the IgG1 subclass do not have a high affinity for protein A. Purification on protein A beads using standard conditions will yield approximately 1/10

    • Purification of mAb (IgG)

        Purification of mAb (IgG) by Chang-Duk Jun, 03/14/2000 Purpose Materials Antibody 7E3 , 2L sup grown in flasks, frozen and thawed overnight. BioRad Affi-Gel Protein A MAPS II Buffers

    • T-Cell Activation Using mAb to CD3

      One of the most common ways to assess T cell activation is to measure T cell proliferation upon in vitro stimulation of T cells via antigen or agonistic antibodies to TCR. This protocol is written as a starting point for examining in vitro proliferation of mouse

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