Phospho-53BP1 (Ser25/29) Antibody产品图

Phospho-53BP1 (Ser25/29) Antib

ody
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  • Cell Signaling Technology已认证
  • USA
  • 2026年05月28日
  • W
  • Rabbit
  • H,Mk
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名:

      Phospho-53BP1 (Ser25/29) Antibody

    • 抗原:

      synthetic phosphopeptide corresponding to residues surrounding Ser25/29 of human 53BP1

    • 应用范围:

      W

    • 宿主:

      Rabbit

    • 库存:

      大量

    • 级别:

      详见MSDS文件

    • 适应物种:

      H,Mk

    • 供应商:

      CST

    • 保质期:

      详见说明书

    • 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:  H=Human  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) Source
    W H Mk Endogenous 450 Rabbit
    Protocols
    Specificity / Sensitivity

    Phospho-53BP1 (Ser25/29) Antibody detects endogenous levels of 53BP1 only when phosphorylated at serine 25/29.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic phosphopeptide corresponding to residues surrounding Ser25/29 of human 53BP1. Antibodies are purified by protein A and peptide affinity chromatography.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from 293 cells, untreated or UV-treated (50 mJ for 2 hours), using Phospho-53BP1 (Ser25/29) Antibody (upper) or 53BP1 Antibody #4937 (lower).

    Background

    p53-binding protein 1 (53BP1) was originally identified as a p53 binding partner that could enhance the transcriptional activity of p53 (1,2). 53BP1 consists of two BRCA1 carboxy terminal (BRCT) domains that allow for binding to p53 and a separate domain responsible for binding to phosphorylated histone H2A.X (3). 53BP1 rapidly translocates to nuclear foci following treatment of cells with ionizing radiation (IR) or radiomimetic agents that cause DNA double strand breaks (DSBs) (4,5). Because of this localization to DSBs and homology to the yeast protein Rad9, a role for 53BP1 in DSB repair has been proposed. Recruitment of 53BP1 to sites of DNA damage has been demonstrated to be independent of ATM, NBS1, and DNA-PK (4) and retention of 53BP1 at DNA breaks requires phosphorylated H2A.X (6). In cells lacking 53BP1, phosphorylation of ATM substrates is reduced, suggesting that 53BP1 is upstream of ATM (7). In response to IR, phosphorylation of 53BP1 at serines 6, 25, 29, and 784 by ATM has been demonstrated, but phosphorylation at these sites is not required for localization of 53BP1 to sites of DSBs (6).

    1. Iwabuchi, K. et al. (1994) Proc. Natl. Acad. Sci. USA 91, 6098-6102.
    2. Iwabuchi, K. et al. (1998) J. Biol. Chem. 273, 26061-26068.
    3. Mochan, T.A. et al. (2004) DNA Repair (Amst) 3, 945-952.
    4. Schultz, L.B. et al. (2000) J. Cell Biol. 151, 1381-1390.
    5. Anderson, L. et al. (2001) Mol. Cell. Biol. 21, 1719-1729.
    6. Ward, I.M. et al. (2003) J. Biol. Chem. 278, 19579-19582.
    7. DiTullio, R.A. et al. (2002) Nat. Cell Biol. 4, 998-1002.
    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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