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- 文献和实验
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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:
872573-93-8
- 规格:
10 mM * 1 mL/5 mg/10 mg/25 mg/50 mg/100 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥825.0 |
|---|---|---|---|
| 规格: | 5 mg | 产品价格: | ¥741.0 |
| 规格: | 10 mg | 产品价格: | ¥1030.0 |
| 规格: | 25 mg | 产品价格: | ¥1800.0 |
| 规格: | 50 mg | 产品价格: | ¥2800.0 |
| 规格: | 100 mg | 产品价格: | ¥4500.0 |
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Ro-3306
CAS No. : 872573-93-8
MCE 国际站:Ro-3306
产品活性:Ro-3306 是一种有效,选择性的 CDK1 抑制剂,对 CDK1,CDK1/cyclin B1 和 CDK2/cyclin E 的 Ki 值为分别为 20 nM,35 nM 和 340 nM。
研究领域:Cell Cycle/DNA Damage | Apoptosis
In Vitro: RO-3306 is an ATP-competitive inhibitor, and inhibits CDK1/cyclin A complexes with Ki of 110 nM. RO-3306 blocks the cell cycle in the G2/M phase of human cancer cells. RO-3306 (4 μM) induces apoptosis in cancer cells. RO-3306 (5 μM) induces G2/M-phase cell cycle arrest and apoptosis of AML cells in a time-dependent manner. RO-3306 treatment significantly increases the percentage of Annexin V-positive cells in G1-phase cells without affecting the cell cycle distribution. RO-3306 enhances p53-mediated apoptosis. RO-3306 cooperates with Nutlin-3 in activating Bax and inducing mitochondrial apoptosis. RO-3306 (5 μM) downregulates antiapoptotic p21, Bcl-2 and survivin protein expression in AML. RO-3306 inhibits p53-induced p21 synthesis. RO-3306 does not inhibit RNA polymerase II CTD phosphorylation. RO-3306 (10 μM) effectively arrests oocyte maturation. RO-3306 reduces the blastocyst formation in oocytes.
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文献和实验inhibitor RO3306. Cells can also be enriched in mitosis by treating with nocodazole and mechanical shake-off. Release of the cells from these blocks enables researchers to follow gene expression and other events through the cell cycle
细胞分裂,竟承担「排毒」的作用?MIT 新发现或为癌症 / 痴呆治疗带来启发
有丝分裂过程中积累。 为了进一步支持溶酶体胞吐在早期有丝分裂中增加的观察,研究人员分别使用 RO-3306(CDK1 抑制剂)和 STLC 将 L1210 细胞同步到 G2 期和有丝分裂早期。STLC 在有丝分裂的干物质变化发生的前中期阻滞细胞。然后他们对细胞表面 LAMP-1 进行免疫标记,并用流式细胞仪进行定量分析,发现被阻滞到早期有丝分裂的细胞表面的 LAMP-1 水平高于被阻滞在 G2 的细胞。 此外,研究人员还检测了细胞周期与 G2 或早期有丝分裂同步后,BaF3 和 THP
有丝分裂过程中积累。 为了进一步支持溶酶体胞吐在早期有丝分裂中增加的观察,研究人员分别使用 RO-3306(CDK1 抑制剂)和 STLC 将 L1210 细胞同步到 G2 期和有丝分裂早期。STLC 在有丝分裂的干物质变化发生的前中期阻滞细胞。然后他们对细胞表面 LAMP-1 进行免疫标记,并用流式细胞仪进行定量分析,发现被阻滞到早期有丝分裂的细胞表面的 LAMP-1 水平高于被阻滞在 G2 的细胞。 此外,研究人员还检测了细胞周期与 G2 或早期有丝分裂同步后,BaF3 和 THP
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