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4°C, protect from light
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货期:1-2天
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MedChemExpress LLC
- CAS号:
1431411-60-7
- 规格:
10 mM * 1 mL/5 mg/10 mg/25 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥1760.0 |
|---|---|---|---|
| 规格: | 5 mg | 产品价格: | ¥1600.0 |
| 规格: | 10 mg | 产品价格: | ¥2600.0 |
| 规格: | 25 mg | 产品价格: | ¥4800.0 |
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SIRT-IN-1
CAS No. : 1431411-60-7
MCE 国际站:SIRT-IN-1
产品活性:SIRT-IN-1 是 SIRT1/2/3 的有效抑制剂,其 IC50 值分别为 15,10,33 μM。
研究领域:Cell Cycle/DNA Damage | Epigenetics
作用靶点:Sirtuin
In Vitro: SIRT-IN-1 (compound 28) is one of the most potent truncated pan SIRT1/ 2/3 inhibitor, the IC50 values are 0.015, 0.010, 0.033 μM, respectively. SIRT-IN-1 (SIRT1/2/3 pan inhibitor) binds identically in the catalytic active site (RMS=0.29 Å), occupying the nicotinamide C-pocket and acetyl lysine substrate channel.
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文献和实验【求助】一句英文怎么翻译?涉及TGFβ-b诱导乙酰化的Foxp3 。谢谢!
,也占用了IL-2的启动子区域,从而抑制IL-2的转录。 背景介绍一下:其实在正常情况下,转录因子Foxp3是启动IL-2的转录,但是使用trichostatin(是一种常用的HDAC(histone deacetylase)抑制剂。Trichostatin A可以通透细胞,选择性抑制HDACs,但不抑制NAD依赖的SIRT系列的deacetylases。)促进Foxp3的表达的同时,也促进了Foxp3的乙酰化,乙酰化的Foxp3增强了其结合在IL-2启动子的能力,但是抑制IL-2的转录
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