重组人乳腺癌易感基因1蛋白/Recombinant human BRCA2 protein, His说明书-分析方法-资讯-生物在线

重组人乳腺癌易感基因1蛋白/Recombinant human BRCA2 protein, His说明书

作者:上海钰博生物科技有限公司 2023-03-30T00:00 (访问量:150)

 Recombinant human BRCA2 protein, His

重组人乳腺癌易感基因1蛋白

英文名称 Recombinant human BRCA2 protein, His
中文名称 重组人乳腺癌易感基因1蛋白
别    名 BRCA 1; 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.   
理论分子量 22.8kDa
性    状 Lyophilized or Liquid
浓    度 >0.5mg/ml
物    种 Human
序    列 210-392/3418
纯    度 >90% as determined by SDS-PAGE
表达系统 E.coli
标签 N-His
缓 冲 液 20mM Tris (pH8.0)
保存条件 Stored at -70℃ or -20℃. Avoid repeated freeze/thaw cycles.
注意事项 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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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