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BRCA1 抗体 (AA 229-335)

This anti-BRCA1 antibody is a 小鼠 单克隆 antibody detecting BRCA1 in IHC 和 ELISA. Suitable for 人. This Primary Antibody has been cited in 1 publication.
产品编号 ABIN1724848
发货至: 中国

Quick Overview for BRCA1 抗体 (AA 229-335) (ABIN1724848)

抗原

See all BRCA1 抗体
BRCA1 (Breast Cancer 1 (BRCA1))

适用

  • 226
  • 39
  • 28
  • 3
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  • 1
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宿主

  • 176
  • 60
  • 2
小鼠

克隆类型

  • 180
  • 58
单克隆

标记

  • 96
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This BRCA1 antibody is un-conjugated

应用范围

  • 125
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Immunohistochemistry (IHC), ELISA

克隆位点

6C6D2
  • 抗原表位

    • 44
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    • 1
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    • 1
    AA 229-335

    原理

    BRCA1 Antibody

    纯化方法

    Purified antibody

    免疫原

    Purified recombinant fragment of human BRCA1 (AA: 229-335) expressed in E. Coli.

    亚型

    IgG1
  • 应用备注

    ELISA: 1/10000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Purified antibody in PBS with 0.05 % sodium azide.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    4 °C,-20 °C

    储存方法

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Muñoz, Laulier, Gunn, Cheng, Robbiani, Nussenzweig, Stark: "RING finger nuclear factor RNF168 is important for defects in homologous recombination caused by loss of the breast cancer susceptibility factor BRCA1." in: The Journal of biological chemistry, Vol. 287, Issue 48, pp. 40618-28, (2012) (PubMed).

  • 抗原

    BRCA1 (Breast Cancer 1 (BRCA1))

    别名

    BRCA1

    背景

    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.


    分子量

    207.7 kDa

    基因ID

    672

    UniProt

    P38398

    途径

    Cell Division Cycle, DNA Damage Repair, Intracellular Steroid Hormone Receptor Signaling Pathway, Positive Regulation of Response to DNA Damage Stimulus
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