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Phospho-C/EBPbeta (Ser105) Ant

ibody (Rat Specific)
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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年12月23日
  • W
  • Rabbit
  • R
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      Phospho-C/EBPbeta (Ser105) Antibody (Rat Specific)

    • 抗原

      synthetic phosphopeptide corresponding to residues surrounding Ser105 of rat C/EBPbeta

    • 应用范围

      W

    • 宿主

      Rabbit

    • 保质期

      详见说明书

    • 级别

      详见MSDS文件

    • 适应物种

      R

    • 供应商

      CST

    • 库存

      大量

    • 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
    Reactivity Key:  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 R Endogenous 41 Rabbit
    Protocols
    Specificity / Sensitivity

    Phospho-C/EBPbeta (Ser105) Antibody (Rat Specific) detects endogenous levels of rat C/EBPbeta only when phosphorylated at serine 105. It does not cross-react with phosphorylated rat C/EBP family members alpha, delta, gamma, epsilon or zeta. It also does not recognize the p20 LIP rat C/EBPbeta isoform.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic phosphopeptide corresponding to residues surrounding Ser105 of rat C/EBPbeta. Antibodies are purified by protein A and peptide affinity chromatography.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from untreated or serum stimulated PC12 cells, using Phospho-C/EBPbeta (Ser105) Antibody (Rat Specific) (A, B) or C/EBPbeta Antibody #3082 (C, D). Nitrocellulose membranes B and D were treated with alkaline phosphatase (CIP) to show the phospho-specificity of Phospho-C/EBPbeta (Ser105) Antibody.

    Background

    CCAAT/enhancer-binding proteins (C/EBPs) are a family of transcription factors critical for cellular differentiation, terminal functions and inflammatory response (1). Six members of the family have been characterized (C/EBPα, -β, -γ, -δ, -ε and -ζ) and are distributed in a variety of tissues (1). There are two forms of C/EBPβ, the 38 kDa liver activating protein (LAP) and the 20 kDa liver inhibitory protein (LIP) which may be products of alternative translation. The 38 kDa LAP protein is a transcriptional activator while LIP may act as an inhibitor of C/EBPβ transcriptional activity (2). Phosphorylation of C/EBPβ at distinct sites stimulates its transcriptional activity (3-5). Phosphorylation at serine 105 of rat C/EBPβ, a unique site only present in the rat sequence, seems essential for rat C/EBPβ activation (6).

    1. Lekstrom-Himes, J. and Xanthopoulos, K.G. (1998) J. Biol. Chem. 273, 28545-28548.
    2. Calkhoven, C.F. et al. (2000) Genes Dev. 14, 1920-1932.
    3. Wegner, M. et al. (1992) Science 256, 370-373.
    4. Trautwein, C. et al. (1993) Nature 364, 544-547.
    5. Nakajima, T. et al. (1993) Proc. Natl. Acad. Sci. USA 90, 2207-2211.
    6. Buck, M. et al. (1999) Mol. Cell 4, 1087-1092.
    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
    • Screening of Antigen-Specific Antibody-Secreting Cells

      Screening of antigen-specific antibody-producing cells is a key step for obtaining antigen-specific monoclonal antibodies. In murine system, hybridoma between B-lymphocytes and myeloma cells is used to screen and produce antigen-specific

    • Rat x Rat Hybridomas

      specific antibody can be obtained from each rat. Furthermore, when nude rats are used for ascites production, the levels of endogenous immunoglobulin can be less than 1 mg/mL.

    • Antibody Targeting of Nanoparticles to Tumor-Specific Receptors: Immunoliposomes

      Immunoliposomes generated by coupling of antibodies to the liposomal surface allow for an active tissue targeting, e.g., through binding to tumor cell-specific receptors. Instead of whole antibodies, single-chain Fv fragments (scFv

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