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XRCC1 Antibody

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年10月22日
  • W, IP, IF-IC
  • Rabbit
  • H
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      XRCC1 Antibody

    • 抗原

      synthetic peptide corresponding to amino acids surrounding Arg300 of human XRCC1

    • 应用范围

      W, IP, IF-IC

    • 宿主

      Rabbit

    • 供应商

      CST

    • 级别

      详见MSDS文件

    • 适应物种

      H

    • 保质期

      详见说明书

    • 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  IP=Immunoprecipitation  IF-IC=Immunofluorescence (Immunocytochemistry)
    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 IP IF-IC H Endogenous 82 Rabbit
    Protocols
    Specificity / Sensitivity

    XRCC1 Antibody detects endogenous levels of total XRCC1 protein.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to amino acids surrounding Arg300 of human XRCC1. Antibodies are purified by protein A and peptide affinity chromatography.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from Jurkat and K562 cells using XRCC1 Antibody.

    IF-IC

    IF-IC

    Confocal immunofluorescent analysis of HeLa cells using XRCC1 Antibody (green). Actin filaments have been labeled with Alexa Fluor® 555 phalloidin (red).

    Background

    The X-ray repair cross complementing protein 1 (XRCC1) is a DNA repair protein important in both single strand break repair and base excision repair following damage from ionizing radiation and alkylating agents (1). XRCC1 acts as a scaffold protein to coordinate DNA abasic site repair through interaction with several other repair proteins (2). At least eight XRCC1 protein partners have been identified, including the polynucleotide kinase PNK (3), DNA ligase III (4,5), poly (ADP-ribose) polymerase (6), and PCNA (7). Mutations and polymorphisms in the XRCC1 gene serve as diagnostic markers and are associated with elevated risk of various forms of cancers (8).

    1. Brem, R. and Hall, J. (2005) Nucleic Acids Res. 33, 2512-2520.
    2. Vidal, A.E. et al. (2001) EMBO J. 20, 6530-6539.
    3. Whitehouse, C.J. et al. (2001) Cell 104, 107-117.
    4. Caldecott, K.W. et al. (1994) Mol. Cell. Biol. 14, 68-76.
    5. Nash, R.A. et al. (1997) Biochemistry 36, 5207-5211.
    6. Masson, M. et al. (1998) Mol. Cell. Biol. 18, 3563-3571.
    7. Fan, J. et al. (2004) Nucleic Acids Res. 32, 2193-2201.
    8. Hu, Z. et al. (2005) Cancer Epidemiol. Biomarkers Prev. 14, 1810-1818.
    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
    • Polymorphisms of DNA Repair Genes: ADPRT, XRCC1, and XPD and Cancer Risk in Genetic Epidemiology

      Many studies have suggested that adenosine diphosphate ribosyl transferase (ADPRT), X-ray repair cross-complementing 1 (XRCC1), and xeroderma pigmentosum complementary group D (XPD) are three major DNA base excision repair (BER) genes

    • Generation of Antibody Molecules Through Antibody Engineering

      been overcome to a large extent using genetic-engineering techniques to produce chimeric mouse/human and completely human antibodies. Such an approach is particularly suitable because of the domain structure of the antibody molecule ( 2 ), where functional

    • The Antibody Molecule

      The importance of antibody molecules was first recognized in the 1890s, when it was shown that immunity to tetanus and diphtheria was caused by antibodies against the bacterial exotoxins (1 ). Around the same time, it was shown that antisera

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