| 货号 | 5032T |
| 同种亚型 | Rabbit IgG |
| 反应种属 | Human,Mouse,Rat,Monkey, |
| 来源宿主 | Rabbit IgG |
| 应用 | WB, IF-IC |
| 目标/特异性 | DNMT1 (D63A6) XP® Rabbit mAb detects endogenous levels of total DNMT1 protein. |
| 使用方法 | WB(1:1000) IF-IC (1:100) |
| 供应商 | CST |
| 灵敏度 | Endogenous |
| 背景 | Methylation of DNA at cytosine residues in mammalian cells is a heritable, epigenetic modification that is critical for proper regulation of gene expression, genomic imprinting and development (1,2). Three families of mammalian DNA methyltransferases have been identified: DNMT1, DNMT2 and DNMT3 (1,2). DNMT1 is constitutively expressed in proliferating cells and functions as a maintenance methyltransferase, transferring proper methylation patterns to newly synthesized DNA during replication. DNMT3A and DNMT3B are strongly expressed in embryonic stem cells with reduced expression in adult somatic tissues. DNMT3A and DNMT3B function as de novo methyltransferases that methylate previously unmethylated regions of DNA. DNMT2 is expressed at low levels in adult somatic tissues and its inactivation affects neither de novo nor maintenance DNA methylation. DNMT1, DNMT3A and DNMT3B together form a protein complex that interacts with histone deacetylases (HDAC1, HDAC2, Sin3A), transcriptional repressor proteins (RB, TAZ-1) and heterochromatin proteins (HP1, SUV39H1), to maintain proper levels of DNA methylation and facilitate gene silencing (3-8). Improper DNA methylation contributes to diseased states such as cancer (1,2). Hypermethylation of promoter CpG islands within tumor suppressor genes correlates with gene silencing and the development of cancer. In addition, hypomethylation of bulk genomic DNA correlates with and may contribute to the onset of cancer. DNMT1, DNMT3A and DNMT3B are over-expressed in many cancers, including acute and chronic myelogenous leukemias, in addition to colon, breast and stomach carcinomas (9-12). |
| 存放说明 | -20C |
| 计算分子量 | 200 |
| 参考文献 | 1 . Hermann, A. et al. (2004) Cell Mol Life Sci 61, 2571-87. 2 . Turek-Plewa, J. and Jagodziński, P.P. (2005) Cell Mol Biol Lett 10, 631-47. 3 . Kim, G.D. et al. (2002) EMBO J. 21, 4183-4195. 4 . Fuks, F. et al. (2001) EMBO J. 20, 2536-2544. 5 . Geiman, T.M. et al. (2004) Biochem. Biophys. Res. Commun. 318, 544-555. 6 . Rountree, M.R. et al. (2000) Nat. Genet. 25, 269-277. 7 . Pradhan, S. and Kim, G.D. (2002) EMBO J. 21, 779-788. 8 . Fuks, F. et al. (2003) Nucleic Acids Res. 31, 2305-2312. 9 . Mizuno, S. et al. (2001) Blood 97, 1172-1179. 10 . Robertson, K.D. et al. (1999) Nucleic Acids Res. 27, 2291-2298. 11 . Xie, S. et al. (1999) Gene 236, 87-95. 12 . Kanai, Y. et al. (2001) Int. J. Cancer 91, 205-212. |
Western blot analysis of extracts from 293 and F9 cells using DNMT1 (D63A6) XP® Rabbit mAb. 使用DNMT1 (D63A6) XP® Rabbit mAb兔单抗，免疫印迹(Western blot)分析293和F9细胞系中DNMT1的蛋白水平。 | |
Confocal immunofluorescent analysis of COS cells using DNMT1 (D63A6) XP® Rabbit mAb (green). Actin filaments were labeled using DY-554 phalloidin (red). 使用DNMT1 (D63A6) XP® Rabbit mAb 兔单抗(绿色)标记，共聚焦免疫荧光分析COS细胞。DY-554 phalloidin标记微丝蛋白(红色)。 |
