| 货号 | 62370S |
| 同种亚型 | Rabbit IgG |
| 反应种属 | Human\Moneky |
| 来源宿主 | Rabbit IgG |
| 应用 | WB, ChIP |
| 目标/特异性 | SMRT (D8D2L) Rabbit mAb recognizes endogenous levels of total SMRT protein. This antibody does not cross-react with NCoR1 protein. |
| 使用方法 | W ChIP |
| 供应商 | CST |
| 灵敏度 | Endogenous |
| 背景 | The most well characterized nuclear receptor corepressors are NCoR1 (nuclear receptor corepressor) and its close paralog NCoR2, also know as SMRT (silencing mediator for retinoic acid and thyroid hormone receptors) (1,2). NCoR1 and SMRT function to transcriptionally silence various unliganded, DNA bound non-steroidal nuclear receptors by serving as a large molecular scaffold that bridges the receptors with multiple chromatin remodeling factors that repress nuclear receptor-mediated gene transcription, in part, through deacetylation of core histones surrounding target promoters. Indeed, the N-terminal portion of NCoR1 and SMRT possess multiple distinct transcriptional repression domains (RDs) responsible for the recruitment of additional components of the corepressor complex such as HDACs, mSin3, GPS2, and TBL1/TBLR1. In between the RDs lies a pair of potent repressor motifs known as SANT motifs (SWI3, ADA2, N-CoR, and TFIIIB), which recruit HDAC3 and histones to the repressor complex in order to enhance HDAC3 activity (3). The C-terminal portion of NCoR1 and SMRT contain multiple nuclear receptor interaction domains (NDs), each of which contains a conserved CoRNR box (or L/I-X-X-I/V-I) motif that allow for binding to various unliganded nuclear hormone receptors such as thyroid hormone (THR) and retinoic acid (RAR) receptors (4,5). |
| 存放说明 | -20C |
| 计算分子量 | 270 |
| 参考文献 | 1 . Chen, J.D. and Evans, R.M. (1995) Nature 377, 454-7. 2 . Hörlein, A.J. et al. (1995) Nature 377, 397-404. 3 . Jones, P.L. and Shi, Y.B. (2003) Curr Top Microbiol Immunol 274, 237-68. 4 . Downes, M. et al. (1996) Nucleic Acids Res 24, 4379-86. 5 . Wong, C.W. and Privalsky, M.L. (1998) Mol Cell Biol 18, 5724-33. |
Western blot analysis of extracts from various cell lines using SMRT (D8S2L) Rabbit mAb. | |
Chromatin immunoprecipitations were performed with cross-linked chromatin from 4 x 106 LS-180 cells treated with calcitriol (10 nM, 3 hr) and either 10 μl of SMRT (D8D2L) Rabbit mAb or 2 μl of Normal Rabbit IgG #2729 using SimpleChIP® Enzymatic Chromatin IP Kit (Magnetic Beads) #9003. The enriched DNA was quantified by real-time PCR using SimpleChIP® Human c-Fos Upstream Primers #25661 and SimpleChIP® Human α-Satellite Repeat Primers #4486. The amount of immunoprecipitated DNA in each sample is represented as signal relative to the total amount of input chromatin, which is equivalent to one. |
