C/EBPα Antibody

C/EBPα Antibody

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年08月31日
  • W, IF-IC
  • Rabbit
  • H,M,R
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    • 详细信息
    • 询价记录
    • 技术资料
    • 抗体英文名

      C/EBPα Antibody

    • 抗原

      synthetic peptide corresponding to the sequence of humanC/EBPα

    • 应用范围

      W, IF-IC

    • 宿主

      Rabbit

    • 适应物种

      H,M,R

    • 供应商

      CST

    • 保质期

      详见说明书

    • 库存

      大量

    • 级别

      详见MSDS文件

    • 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
    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 R Endogenous 42, 28 Rabbit
    Protocols
    Specificity / Sensitivity

    C/EBPα Antibody detects endogenous levels of total C/EBPα protein.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to the sequence of humanC/EBPα. Antibodies are purified by protein A and peptide affinity chromatography.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from THP1 and NIH/3T3-L1 cells using C/EBPα Antibody.

    IF-IC

    IF-IC

    Confocal immunofluorescent image of 3T3-L1 cells labeled with C/EBPalpha Antibody (green) showing nuclear localization in differentiated cells.

    Background

    CCAAT/enhancer-binding proteins (C/EBPs) are a family of transcription factors that are critical for cellular differentiation, terminal function, and inflammatory response (1). Six members of the family have been characterized (C/EBPα, β, δ, γ, ε, and ζ) and are distributed in a variety of tissues (1). Translation from alternative start codons results in two isoforms of C/EBPα (p42 and p30), which are both strong transcriptional activators (2). It has been reported that insulin and insulin-like growth factor-I stimulate the dephosphorylation of C/EBPα, which may play a key role in insulin-induced repression of GLUT4 transcription (3). Phosphorylation of C/EBPα at Thr222, Thr226, and Ser230 by GSK-3 seems to be required for adipogenesis (4).

    1. Lekstrom-Hims, J. and Xanthopoulos, K.G. (1998) J. Biol. Chem. 273, 28545-28548.
    2. Lin, F. et al. (1993) Proc. Natl. Acad. Sci. USA 90, 9606-9610.
    3. Hemati, N. et al. (1997) J. Biol. Chem. 272, 25913-25919.
    4. Ross, S.E. et al. (1999) Mol. Cell. Biol. 19, 8433-8441.
    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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