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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; 4°C, 2 years. In solvent: -80°C, 6 months; -20°C, 1 month.
- 英文名：
Antibiotic AM-2282; STS; AM-2282
- 库存：
货期：1-2天
- 供应商：
MedChemExpress LLC
- CAS号：
62996-74-1
- 规格：
10 mM * 1 mL/2 mg/5 mg/10 mg/25 mg/50 mg
| 规格： | 10 mM * 1 mL | 产品价格： | ￥1673.0 |
|---|---|---|---|
| 规格： | 2 mg | 产品价格： | ￥900.0 |
| 规格： | 5 mg | 产品价格： | ￥1630.0 |
| 规格： | 10 mg | 产品价格： | ￥2600.0 |
| 规格： | 25 mg | 产品价格： | ￥4650.0 |
| 规格： | 50 mg | 产品价格： | ￥6950.0 |
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Staurosporine
CAS No. : 62996-74-1
MCE 国际站：Staurosporine
产品活性：Staurosporine 是一种有效，ATP 竞争性的，非选择性蛋白激酶抑制剂，抑制 PKC，PKA，c-Fgr，和 Phosphorylase kinase 的 IC50 分别为 6 nM，15 nM，2 nM，3 nM。Staurosporine 也抑制 TAOK2，IC50 值 3 μM。Staurosporine 是一个凋亡诱导剂。
研究领域：Epigenetics | TGF-beta/Smad | Stem Cell/Wnt | Apoptosis | Anti-infection
作用靶点：PKC | PKA | Apoptosis | Bacterial | Fungal | Antibiotic
In Vitro: Staurosporine, widely used as a protein kinase C (PKC) inhibitor with a broad spectrum of activity, is an alkaloid which can be isolated from the culture broth of Streptomyces staurospores. MC3T3E-1 osteoblasts, expose to Staurosporine (100 nM) for 12 h, release an amount of LDH (12.4±3.1%) that is similar to that release by the control cells(10.0±2.4%), indicating the relative absence of lytic death, which occurs in necrosis. In addition, treatment with Staurosporine (100 nM) results in morphological changes, characteristic of apoptosis: a brightblue fluorescent condensed nuclei seen through a fluorescence microscope after Hoechst 33258-staining, and a reduction of cell volume.
In Vivo: The inhibitory effect of Staurosporine is statistically significant at around Wk 10 of tumor promotion. Although statistically significant inhibition is not obtained with 10 ng of Staurosporine in later weeks of the experiment, a decreasing tendency in the percentages of tumor bearing mice and in average numbers of tumors per mouse is apparent. Thus, Staurosporine slightly inhibits tumor promotion of Teleocidin, even at the dose at which Staurosporine itself induced tumors. Staurosponne (0.05 and 0.1 mg/kg intraperitoneal) attenuates the impaired perlormance of water maze and passive avoidance tasks, even though the drug administration began 2 weeks after the lesion. Moreover, Staurosporine (0.1 mg/kg) partially reversed the decrease of choline acetyltransferase activity in the fronto-parietal cortex induced by basal forebrain-lesion. These results suggest that Staurosporine attenuates impairment of learning through reversal of damage to cholinergic neurons induced by basal forebrain-lesion.
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文献和实验with any kinase inhibitor as selectivity function can be synthesized. We here used staurosporine as the selectivity function because it targets and, therefore, allows profiling a broad range of kinases (Romano and Giordano, Cell Cycle 7:3364–3668, 2008
原代心肌细胞的培养及实验方案 取出生后0~24 h C57BL/6cr小鼠心脏，按改良的Lader方法进行细胞的分离。 获取博动的心脏迅速放置于无Ca2+、Mg2+的Hank’s平衡液中。剪碎心脏，放置在4℃条件下100 g/L的Trypsin溶液中消化16~18 h，用Trypsin抑制剂中止消化。然后在37℃下，用胶原酶Ⅱ于CO2培养箱内，在摇床上继续孵化消化45~60 min，最后用70 μm直径尼龙过滤网过滤获取心肌细胞，用含有25 mmol/L HCO3-，100 mL/L
(GIBCO-BRL) according to the manufacturer's recommendations. Following transfection, the cells were allowed to recover in complete medium for 16 h and were then either left untreated or an apoptotic stimulus (800 ng/ml staurosporine; Sigma) (22 ,23
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