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BRCA1 Mouse Monoclonal Antibod

y [Clone ID: LBI2A5]
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  • ¥690 - 2025
  • Leading Biology
  • 美国
  • 2025年07月14日
  • WB 1:2000
  • Mouse
  • Human
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 靶点

      BRCA1

    • 浓度

      1 mg/ml

    • 应用范围

      WB 1:2000

    • 宿主

      Mouse

    • 适应物种

      Human

    • 保质期

      1-2年

    • 供应商

      安诺伦(北京)生物科技有限公司

    • 标记物

      Unconjugated

    • 克隆性

      Monoclonal Antibody

    • 保存条件

      Store at +4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

    • 形态

      PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.

    • 亚型

      IgG1

    • 免疫原

      Human recombinant protein fragment corresponding to amino acids 1151-1473 of human BRCA1 (NP_009225) produced in E.coli.

    • 规格

      100 ul/30 ul

    规格:100 ul产品价格:¥2025.0
    规格:30 ul产品价格:¥690.0
    别名:BRCAI; BRCC1; BROVCA1; FANCS; IRIS; PNCA4; PPP1R53; PSCP; RNF53

    产品概述:BRCA1 mouse monoclonal antibody, clone LBI2A5

    总结:This gene encodes a nuclear phosphoprotein that plays a role in maintaining genomic stability, and it also acts as a tumor suppressor. The encoded protein combines with other tumor suppressors, DNA damage sensors, and signal transducers to form a large multi-subunit protein complex known as the BRCA1-associated genome surveillance complex (BASC). This gene product associates with RNA polymerase II, and through the C-terminal domain, also interacts with histone deacetylase complexes. This protein thus plays a role in transcription, DNA repair of double-stranded breaks, and recombination. Mutations in this gene are responsible for approximately 40% of inherited breast cancers and more than 80% of inherited breast and ovarian cancers. Alternative splicing plays a role in modulating the subcellular localization and physiological function of this gene. Many alternatively spliced transcript variants, some of which are disease-associated mutations, have been described for this gene, but the full-length natures of only some of these variants has been described. A related pseudogene, which is also located on chromosome 17, has been identified. [provided by RefSeq, May 2009]

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