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DNA-PK Antibody

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年09月01日
  • W
  • Rabbit
  • H
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      DNA-PK Antibody

    • 抗原

      synthetic peptide corresponding to amino acids near the carboxy-terminus of human DNA-PKcs

    • 应用范围

      W

    • 宿主

      Rabbit

    • 级别

      详见MSDS文件

    • 库存

      大量

    • 适应物种

      H

    • 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

      40 ul (4 western blots)/100 ul (10 western blots)/carrier free & custom formulation / quantity

    规格:产品价格:¥请询价
    规格:40 ul (4 western blots)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
    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 Endogenous 450 Rabbit
    Protocols
    Specificity / Sensitivity

    DNA-PK Antibody detects endogenous levels of DNA-PK protein.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to amino acids near the carboxy-terminus of human DNA-PKcs. Antibodies are purified by protein A and peptide affinity chromatography.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from M059K (DNA-PK wildtype) and M059J (DNA-PK deficient) cells, using DNA-PK Antibody.

    Background

    DNA-dependent protein kinase (DNA-PK) is an important factor in the repair of double-stranded breaks in DNA. Cells lacking DNA-PK or in which DNA-PK is inhibited fail to show proper nonhomologous end-joining (NHEJ) (1-7). DNA-PK is composed of two DNA-binding subunits (Ku70 and Ku86) and one 450 kDa catalytic subunit (DNA-PKcs) (8). It is thought that a heterodimer of Ku70 and Ku86 binds to double-stranded DNA broken ends before DNA-PKcs binds and is activated (1,9). Activated DNA-PKcs is a serine/threonine kinase that has been shown to phosphorylate a number of proteins in vitro , including p53, transcription factors, RNA polymerase, and Ku70/Ku86 (10,11). DNA-PKcs autophosphorylation at multiple sites, including Thr2609 and Ser2056, results in an inactivation of DNA-PK kinase activity and NHEJ ability (12,13). It has been demonstrated, however, that DNA-PK preferentially phosphorylates substrates before it autophosphorylates, suggesting that DNA-PK autophosphorylation may play a role in disassembly of the DNA repair machinery (14,15). Autophosphorylation at Thr2609 has also been shown to be required for DNA-PK-mediated double strand break repair, and phosphorylated DNA-PK co-localizes with H2A.X and 53BP1 at sites of DNA damage (16). Phosphorylation at Ser2056 occurs in response to double-stranded DNA breaks and ATM activation (17).

    1. Gottlieb, T.M. and Jackson, S.P. (1993) Cell 72, 131-142.
    2. Hartley, K. O. et al. (1995) Cell 82, 840-856.
    3. Rosenzweig, K. E. et al. (1997) Clin. Cancer Res. 3, 1149-1156.
    4. Jackson, S.P. and Jeggo, P.A. (1995) Trends Biochem. Sci. 20, 412-415.
    5. Roth, D. B. et al. (1995) Curr. Biol. 5, 496-499.
    6. Baumann, P. and West, S.C. (1998) Proc. Natl. Acad. Sci. USA 95, 14066-14070.
    7. Chen, S. et al. (2001) J. Biol. Chem. 276, 24323-24330.
    8. Jeggo, P.A. (1997) Mutat. Res. 384, 1-14.
    9. Suwa, A. et al. (1994) Proc. Natl. Acad. Sci. USA 91, 6904-6908.
    10. Anderson, C.W. and Lees-Miller, S.P. (1992) Crit. Rev. Eukaryot. Gene Expr. 2, 283-314.
    11. Kuhn, A. et al. (1995) Genes Dev. 9, 193-203.
    12. Chan, D.W. and Lees-Miller, S.P. (1996) J. Biol. Chem. 271, 8936-8941.
    13. Douglas, P. et al. (2002) Biochem. J. 368, 243-251.
    14. Lees-Miller, S. P. et al. (1992) Mol. Cell. Biol. 12, 5041-5049.
    15. Jackson, S. P. et al. (1990) Cell 63, 155-165.
    16. Chan, D. W. et al. (2002) Genes Dev. 16, 2333-2338.
    17. Yajima, H. et al. (2009) J Mol Biol 385, 800-10.
    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
    • Mol Cell:杨薇等揭示 DNA-PK 的激活机制以及自磷酸化对 NHEJ 通路的重要作用​

      DNA 双链断裂可由外在因素(电离辐射和活性氧等)或内在因素(DNA 复制错误和 V(D)J 重组等)造成,从而激发 DNA 损伤应答,包括 DNA 修复、细胞周期调控、细胞衰老和细胞凋亡等。 DNA 损伤应答由 PIKK(phosphoinositide-3-kinase-related kinase)家族蛋白激酶催化下游蛋白的磷酸化而启动,包括 DNA-PKDNA 依赖性蛋白激酶)、ATM(Ataxia Telangiectasia Mutated)和 ATR(ATM-Related

    • 外泌体分离:超速离心法 PK 试剂盒法,谁赢了?

      一、什么是外泌体? 外泌体(Exosomes)是大小为 30-150 nm、呈茶托状的细胞外囊泡(Extracellular vesicles, EVs),广泛存在于细胞培养上清及各种体液中,包括血液、淋巴液、唾液、尿液、精液、乳汁等。 几乎所有细胞都可以分泌外泌体,但是外泌体来源不同,其内部装载的 RNA、蛋白质、脂类等重要物质在数量和丰度上有很大差异。 二、外泌体的作用和功能 外泌

    • Fusion Proteins with Improved PK

      Small recombinant antibody formats are rapidly cleared from circulation. The coupling of these molecules to human serum albumin (HSA) is an efficient strategy to prolong their in vivo half-life. Two methods are described in this chapter

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