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BRCA1 抗体 (AA 443-472)

This anti-BRCA1 antibody is a 兔 多克隆 antibody detecting BRCA1 in WB 和 ELISA. Suitable for 人.
产品编号 ABIN3030201
发货至: 中国

Quick Overview for BRCA1 抗体 (AA 443-472) (ABIN3030201)

抗原

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

适用

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宿主

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克隆类型

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多克隆

标记

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This BRCA1 antibody is un-conjugated

应用范围

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Western Blotting (WB), ELISA
  • 抗原表位

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    AA 443-472

    纯化方法

    Antigen affinity purified

    免疫原

    A portion of amino acids 443-472 from the human protein was used as the immunogen for this BRCA1 antibody.

    亚型

    Ig Fraction
  • 应用备注

    Titration of the BRCA1 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    In 1X PBS pH 7.4 with 0.09 % 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

    -20 °C

    储存方法

    Aliquot the BRCA1 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • 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. [provided by RefSeq].

    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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