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Recombinant human BRCA1 protein (C-His-Tag) (bs-10856P)

Recombinant human BRCA1 protein (C-His-Tag) (bs-10856P)

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Recombinant human BRCA1 protein (C-His-Tag)

英文名称Recombinant human BRCA1 protein (C-His-Tag)
中文名称重组人乳腺癌易感基因1蛋白
别    名BRCA 1; BRCA1; BRCA1/BRCA2 containing complex subunit 1; BRCA1/BRCA2-containing complex, subunit 1; BRCA1_HUMAN; BRCAI; BRAC 1; BRCA 1; BRCC 1; BRCC1; Breast Cancer 1; Breast Cancer 1 Early Onset; Breast cancer type 1 susceptibility protein; Breast and ovarian cancer susceptibility protein 1; Breast Ovarian Cancer Susceptibility; IRIS; Papillary Serous Carcinoma Of The Peritoneum; PSCP; RING finger protein 53; BROVCA1; IRIS; PNCA4; PPP1R53; Protein phosphatase 1 regulatory subunit 53; RNF53; BAP1. 


分 子 量24.5kDa
性    状Lyophilized or Liquid
浓    度1mg/ml
种属同源Human
序    列1661-1863/1863aa
产品来源基因工程表达
分    类重组蛋白
纯化方法亲和层析
产品应用Immunology research 
保存条件Stored at -70℃ or -20℃. Avoid repeated freeze/thaw cycles.
产品介绍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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