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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
Powder: -20°C, 3 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:
136194-77-9
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥1777.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥800.0 |
| 规格: | 5 mg | 产品价格: | ¥1615.0 |
| 规格: | 10 mg | 产品价格: | ¥2580.0 |
| 规格: | 25 mg | 产品价格: | ¥4053.0 |
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Go6976
CAS No. : 136194-77-9
MCE 国际站:Go6976
产品活性:Go6976 是蛋白激酶C (PKC) 的一个抑制剂,其 IC50 值为20 nM。
研究领域:Epigenetics | TGF-beta/Smad | Anti-infection
作用靶点:PKC | Influenza Virus
In Vitro: Go6976 is a potent inhibitor of PKC in vitro (IC50 is 20 nM. This compound is structurally related to staurosporine, which is the most potent PKC inhibitor. UCN-01 is originally identified as a PKC inhibitor. Surprisingly, Go6976 is found to abrogate S and G2 arrest. Dose-response studies reveal that 30 nM Go6976 is sufficient to cause abrogation of S-phase arrest in 6 h and abrogation of G2 arrest followed by lethal mitosis in 24 h. Incubation of cells with 100 nM Go6976 is sufficient to cause complete abrogation of S and G2 arrest at 6 and 24 h, respectively, which is only slightly less potent than in bovine serum. Incubation of cells with UCN-01 or Go6976 alone do not decrease viability compared with control at the concentrations used. Incubation of cells with 5 ng/mL SN38 result in cytostasis, and addition of 50 nM UCN-01 or 100 nM Go6976 to arrested MDA-MB-231 cells cause a dramatic decrease in viable cell number by 96 h.
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文献和实验Evaluation of the Fate of rAAV Genomes Following In Vivo Administration
and concatemeric episomal forms in skeletal muscle and liver (Schnepp et al. J Virol 77: 3495–3504, 2003; Penaud-Budloo et al. J Virol 82: 7875–7885, 2008; Nakai et al. J Virol 75: 6969–6976, 2001). Moreover, in nonhuman primate skeletal muscle, it has been shown
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