INH6 ≥98%
| 货号 | 规格 | 价格 | 上海 | 北京 | 珠海 | 重庆 | 武汉 | 购买数量 |
|---|---|---|---|---|---|---|---|---|
S80005-10mg促销 |
≥98% | ￥462.00 ￥416.00 |
10 | 3 | - | - | - |
|
S80005-25mg促销 |
≥98% | ￥1030.00 ￥926.00 |
4 | - | - | - | - |
|
S80005-50mg促销 |
≥98% | ￥1480.00 ￥1330.00 |
2 | - | - | - | - |
|
S80005-100mg促销 |
≥98% | ￥2410.00 ￥2160.00 |
1 | - | - | - | - |
|
| 产品描述： | INH6, an effective Hec1 inhibitor, selectively disrupts the Hec1/Nek2 interaction and induces chromosome mis-alignment. | ||||||||||||||||||||
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| 靶点： | Apoptosis;Microtubule Associated;Apoptosis;MicrotubuleAssociated | ||||||||||||||||||||
| 细胞实验： | Standard XTT assays with a four-day drug treatment procedure are performed to measure the dose-dependent cytotoxicity of INH analogs in cultured cells. Triplicate sets are measured and compiled for final data presentation. The assay is performed by using a commercial kit following the instructions. In principle, cells are plated on 96-well dishes one day before the drug treatment, followed by drug treatment on day 2 and XTT assay on day 5 after drug addition. The absorption at 595 nm is measured with a plate reader and converted to cell survival percentages in comparison to mock treated groups.(Only for Reference) | ||||||||||||||||||||
| 参考文献： | 1. Qiu XL, et al. J Med Chem. 2009, 52(6), 1757-1767. | ||||||||||||||||||||
| 溶解性： | Soluble in DMSO、Ethanol | ||||||||||||||||||||
| 保存条件： | -20℃ | ||||||||||||||||||||
| 配置溶液浓度参考： |
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| 注意： | 部分产品我司仅能提供部分信息，我司不保证所提供信息的权威性，仅供客户参考交流研究之用。 |
参考文献
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