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BRCA1 抗体

BRCA1 适用: 人, 小鼠 IHC, IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6566504
发货至: 中国
  • 抗原 See all BRCA1 抗体
    BRCA1 (Breast Cancer 1 (BRCA1))
    适用
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    人, 小鼠
    宿主
    • 162
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    克隆类型
    • 166
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    多克隆
    标记
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    This BRCA1 antibody is un-conjugated
    应用范围
    • 127
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    Immunohistochemistry (IHC), Immunofluorescence (IF)
    纯化方法
    Affinity purification
    免疫原
    A synthetic peptide of human BRCA1 (NP_009225.1).
    亚型
    IgG
    Top Product
    Discover our top product BRCA1 Primary Antibody
  • 应用备注
    IHC 1:50-1:200 IF 1:20-1:50
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    缓冲液
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    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
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    BRCA1 (Breast Cancer 1 (BRCA1))
    别名
    BRCA1 (BRCA1 产品)
    别名
    BRCAI antibody, BRCC1 antibody, BROVCA1 antibody, IRIS antibody, PNCA4 antibody, PPP1R53 antibody, PSCP antibody, RNF53 antibody, iris antibody, pscp antibody, brcai antibody, brcc1 antibody, rnf53 antibody, brca1 antibody, BRCA1 antibody, LOC100224649 antibody, BRCA1, DNA repair associated antibody, breast cancer 1 antibody, breast cancer 1, early onset antibody, breast cancer 1 L homeolog antibody, BRCA1 antibody, brca1 antibody, LOC755086 antibody, Brca1 antibody, brca1.L antibody
    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

    Observed_MW: 85kDa

    Calculated_MW: 7kDa/78-85kDa/202-210kDa

    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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