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JMS-17-2 是选择性CX3CR1拮抗剂(IC50:0.32 nM),能够抑制乳腺癌细胞的转移和定植。
JMS-17-2 是选择性CX3CR1拮抗剂(IC50:0.32 nM),能够抑制乳腺癌细胞的转移和定植。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 329 | 现货 | |
2 mg | ¥ 472 | 现货 | |
5 mg | ¥ 745 | 现货 | |
10 mg | ¥ 1,230 | 现货 | |
25 mg | ¥ 2,110 | 现货 | |
50 mg | ¥ 3,320 | 现货 | |
100 mg | ¥ 4,750 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 822 | 现货 |
产品描述 | JMS-17-2 is a potent and selective antagonist of CX3CR1( IC50 : 0.32 nM). |
靶点活性 | CX3CR1:0.32 nM |
动物实验 | SKBR3 human breast cancer cells were serum starved for four hours before being exposed to 50nM recombinant human FKN for 5 minutes, with or without previous incubation with either a CX3CR1 neutralizing antibody used at 15μg/ml or the JMS-17-2 antagonist (10nM) for 30 minutes at 37 ℃. |
分子量 | 419.95 |
分子式 | C25H26ClN3O |
CAS No. | 1380392-05-1 |
存储 | store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||
溶解度信息 | DMSO: 11 mg/mL (26.19 mM) | |||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||
DMSO
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