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- 保存条件:
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
1374601-40-7
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg/50 mg/100 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥489.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥247.0 |
| 规格: | 5 mg | 产品价格: | ¥538.0 |
| 规格: | 10 mg | 产品价格: | ¥868.0 |
| 规格: | 25 mg | 产品价格: | ¥1780.0 |
| 规格: | 50 mg | 产品价格: | ¥2860.0 |
| 规格: | 100 mg | 产品价格: | ¥4270.0 |
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BRD4770
CAS No. : 1374601-40-7
MCE 国际站:BRD4770
产品活性:BRD4770 是一种组蛋白甲基转移酶 G9a 抑制剂。BRD4770 可抑制 H3K9 的二甲基和三甲基化,EC50 为 5 µM,对 H3K27me3,H3K36me3,H3K4me3 和 H3K79me3 几乎没有影响。BRD4770 可以激活共济失调毛细血管扩张突变 (ATM) 途径并诱导细胞衰老。
研究领域:Epigenetics
作用靶点:Histone Methyltransferase
In Vitro: BRD4770 (0-20 µM; 72 hours; PANC-1 cells) treatment reduces the number of cells after 72 h.
BRD4770 (2.5-5 µM; 24 hours; PANC-1 cells) treatment decreases H3K9 trimethylation level by 23% in PANC-1 cells.
BRD4770 induces a senescent phenotype in a pancreatic cancer cell line. BRD4770 also inhibits both anchorage-dependent and -independent cell proliferation and induces G2/M cell-cycle arrest. BRD4770 activates the ataxia telangiectasia mutated (ATM) pathway without inducing DNA damage, while the ataxia telangiectasia and Rad3-related protein (ATR) pathway is not affected.
BRD4770 also induces increased levels of lysine acetylation in cells without inhibiting histone deacetylases.
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文献和实验://www.dxy.cn/bbs/post/view?bid=68&id=8795625&sty=1&tpg=6&age=0 39 【求助】胞内蛋白做ELISA,标本需特殊处理吗? http://www.dxy.cn/bbs/post/view?bid=68&id=8790004&sty=1&tpg=6&age=0 40 【求助】请教Brd渗入法测定细胞的增殖 http://www.dxy.cn/bbs/post/view?bid=68&id=8789895&sty=1&tpg=6&age
Using MODELTEST and PAUP* to Select a Model of Nucleotide Substitution
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Overview of the Measurement of Lipids and Lipoproteins in Mice
.W., and Oda, M.N. 2008. The interplay between size, morphology, stability, and functionality of high‐density lipoprotein subclasses. Biochemistry 47:4770‐4779. Chen, C.H
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