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- 文献和实验
- 技术资料
- 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:
1957203-01-8
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥2893.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥971.0 |
| 规格: | 5 mg | 产品价格: | ¥2488.0 |
| 规格: | 10 mg | 产品价格: | ¥4350.0 |
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YKL-5-124
CAS No. : 1957203-01-8
MCE 国际站:YKL-5-124
产品活性:YKL-5-124 是一种有效的、选择性不可逆 CDK7 共价抑制剂,对 CDK7 和 CDK7/Mat1/CycH 的 IC50 分别为 53.5 nM 和 9.7 nM。YKL-5-124 对 CDK7 的选择性比 CDK9 和 CDK2 高 100 倍以上,并且对 CDK12 和 CDK13 没有活性。YKL-5-124 诱导强烈的细胞周期停滞,并抑制 E2F 驱动的基因表达,并且对 RNA 聚合酶 II 磷酸化状态几乎没有影响。
研究领域:Cell Cycle/DNA Damage
作用靶点:CDK
In Vitro: YKL-5-124 (0-2000 nM; 72 hours; HAP1 cells) treatment causes a dose-dependent increase in G1- and G2/M-phase cells and a corresponding loss of S-phase cells.
YKL-5-124 (0-2000 nM; 24 hours; HAP1 WT cells) treatment inhibits CDK1 T-loop phosphorylation, and to a lesser extent CDK2 T-loop phosphorylation in a concentration-dependent fashion.
Treatment of cells with YKL-5-124 as a competitor at a concentration of about 30 nM blocks pull-down of CDK7-cyclin H but has no effect on the pull-down of cyclin K-CDK12/13 in HAP1 cells. Treatment with 100 nM YKL-5-124 reduces CDK7-cyclin H binding to bioTHZ1 by >50% at 30 min.
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文献和实验【交流】MIRNA(microRNA)检测实验流程(加polyA法
MIMAT0000422 hsa-miR-124 733 hsmq-0033_01 MIMAT0000443 hsa-miR-125a-5p 774 hsmq-0034_01 MIMAT0000423 hsa-miR-125b 755 hsmq-0035_01 MIMAT0000429 hsa-miR-137 766 hsmq-0036_01 MIMAT0000250 hsa-miR-139-5p 757 hsmq-0037_01
【分享】MIRNA(microRNA)检测实验流程(加polyA法) (2011
-miR-124 73 3 hsmq-0033_01 MIMAT0000443 hsa-miR-125a-5p 77 4 hsmq-0034_01 MIMAT0000423 hsa-miR-125b 75 5 hsmq-0035_01 MIMAT0000429 hsa-miR-137 76 6 hsmq-0036_01 MIMAT0000250 hsa-miR-139-5p 75 7 hsmq-0037_01 MIMAT0000437
MIRNA(microRNA)检测实验流程(加polyA法)
1 hsmq-0031_01 MIMAT0000069 has-miR-16 75 2 hsmq-0032_01 MIMAT0000422 hsa-miR-124 73 3 hsmq-0033_01
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