| 货号 | 6623S |
| 描述 | SignalSilence® Bub1b siRNA I from Cell Signaling Technology (CST) allows the researcher to specifically inhibit Bub1b expression using RNA interference, a method whereby gene expression can be selectively silenced through the delivery of double stranded RNA molecules into the cell. All SignalSilence® siRNA products from CST are rigorously tested in-house and have been shown to reduce target protein expression by western analysis.Cell Signaling Technology (CST) 公司的SignalSilence® Bub1b siRNA 帮助研究人员使用RNA干扰技术特异性抑制Bub1b表达，该技术通过向细胞内导入双链RNA分子以选择性的抑制某些基因的表达。所有CST公司的SignalSilence® siRNA都经过了严格的内部测试，western分析显示能够能够降低目标蛋白的表达。Quality Control |
| 反应种属 | Human |
| 应用 | TFN |
| 供应商 | CST |
| 背景 | The Mitotic Checkpoint Complex (MCC), which contains Bub1, Bub1b, Bub3, Mad2, and Cdc20, controls chromosome segregation and monitors kinetochore-microtubule interactions (1). During mitosis, the MCC complex inhibits the ubiquitin ligase activity of the Anaphase Promoting Complex/Cyclosome (APC/C), thereby preventing cells with unaligned chromosomes from prematurely entering anaphase (2). Research studies have shown that Bub1b and Bub1 kinases are mutated in several types of human malignancies including hematopoietic, colorectal, lung, and breast cancers (3). Biallelic mutations in Bub1b have been found in mosaic variegated aneuploidy syndrome and premature chromatid separation syndrome (4). Bub1b mouse germline knockouts are embryonic lethal with heterozygous animals displaying genetic instability, early aging phenotypes, and increased cancer susceptibility (5). Bub3 binds both Bub1 and Bub1b, facilitating their recruitment to kinetochores (6), and is required for functional microtubule-kinetochore interactions (7).有丝分裂检验点复合物（MCC），包括Bub1, Bub1b, Bub3, Mad2, 和Cdc20, 控制染色体分离并监控着丝粒微管相互作用（1）。在有丝分裂期，MCC复合物抑制细胞分裂后期促进复合物/ Cyclosome（APC/C）的泛素连接酶功能，从而防止未成熟折叠形成染色体的细胞进入有丝分裂后期（2）。研究证实在包括血癌，大肠癌，肺癌，乳腺癌再累的多种人类恶性肿瘤中都发现Bub1b和Bub1激酶发生了突变（3）。mosaic variegated aneuploidy 综合征和 premature chromatid separation 综合征病人也发现Bub1b基因存在双灯位基因突变（4）。在小鼠生殖细胞中敲除Bub1b基因是胚胎致死的，杂合子动物则表现出遗传不稳定性，早衰及患癌的风险上升等特点（5）。Bub3能够与Bub1和Bub1b结合，促进它们集中到着丝粒（6），在微管-着丝粒的相互作用过程中，Bub3也是不可或缺的（7）。 |
| 存放说明 | -20C |
| 参考文献 | Fukagawa, T. (2008) Front Biosci 13, 2705-13. Chen, R.H. (2007) J Biomed Sci 14, 475-9. Dai, W. et al. (2004) Cancer Res 64, 440-5. Kops, G.J. et al. (2005) Nat Rev Cancer 5, 773-85. Baker, D.J. et al. (2004) Nat Genet 36, 744-9. Taylor, S.S. et al. (1998) J Cell Biol 142, 1-11. Logarinho, E. et al. (2008) Mol Biol Cell 19, 1798-813. |
Western blot analysis of extracts from HeLa cells, transfected with 100 nM SignalSilence® Control siRNA (Unconjugated) #6568 (-), SignalSilence® Bub1b siRNA I (+), or SignalSilence® Bub1b siRNA II #12150 (+), using Bub1b (D32E8) Rabbit mAb #5421 (upper) or β-Actin (D6A8) Rabbit mAb #8457 (lower). The Bub1b (D32E8) Rabbit mAb confirms silencing of Bub1b expression, while the β-Actin (D6A8) Rabbit mAb is used as a loading control.转染100 nM SignalSilence® 对照 siRNA (未标记) #6568 (-), SignalSilence® Bub1b siRNA I (+), 或SignalSilence® Bub1b siRNA II #12150 (+)的HeLa细胞提取物，使用Bub1b (D32E8) Rabbit mAb #5421 (上) 或 β-Actin (D6A8) Rabbit mAb #8457 (下)进行western blot分析。Bub1b (D32E8) Rabbit mAb证实Bub1b的表达受抑制，β-Actin (D6A8) Rabbit mAb用于确认上样量一致。 |
