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Cell-permeable calmodulin (CaM) agonist that binds to the EF-hand/Ca2+-binding site. Activates phosphodiesterase in the absence of Ca2+ and inhibits Ca2+-mediated cytotoxicity and apoptosis (IC50 = 33 μM).

Cell-permeable calmodulin (CaM) agonist that binds to the EF-hand/Ca2+-binding site. Activates phosphodiesterase in the absence of Ca2+ and inhibits Ca2+-mediated cytotoxicity and apoptosis (IC50 = 33 μM).
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 1,260 | 待询 | |
| 5 mg | ¥ 4,930 | 待询 | |
| 10 mg | ¥ 8,360 | 待询 | |
| 25 mg | ¥ 14,300 | 待询 | |
| 50 mg | ¥ 21,600 | 待询 | |
| 100 mg | ¥ 32,800 | 待询 |
| 产品描述 | Cell-permeable calmodulin (CaM) agonist that binds to the EF-hand/Ca2+-binding site. Activates phosphodiesterase in the absence of Ca2+ and inhibits Ca2+-mediated cytotoxicity and apoptosis (IC50 = 33 μM). |
| 分子量 | 881.08 |
| 分子式 | C44H68N10O9 |
| CAS No. | 261969-05-5 |
| 密度 | no data available |
| Sequence Short | VKFGVGFK |
| 存储 | keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | ||||||||||
| 溶解度信息 | H2O: 1 mg/mL (1.13 mM), Sonication is recommended. | ||||||||||
溶液配制表 | |||||||||||
H2O
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以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
对于不同动物的给药剂量换算,您也可以参考 更多