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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
零下80~20°C
- 保质期:
Powder: -20°C for 3 years In solvent: -80°C for 2 years
- 英文名:
SCH772984
- 库存:
10
- 供应商:
TargetMol
- CAS号:
942183-80-4
- 规格:
100 mg/500 mg/25 mg/200 mg/50 mg/1 mg/5 mg/2 mg/10 mg/1 mL
| 规格: | 100 mg | 产品价格: | ¥5930.0 |
|---|---|---|---|
| 规格: | 500 mg | 产品价格: | ¥11800.0 |
| 规格: | 25 mg | 产品价格: | ¥2880.0 |
| 规格: | 200 mg | 产品价格: | ¥7850.0 |
| 规格: | 50 mg | 产品价格: | ¥4170.0 |
| 规格: | 1 mg | 产品价格: | ¥582.0 |
| 规格: | 5 mg | 产品价格: | ¥1150.0 |
| 规格: | 2 mg | 产品价格: | ¥848.0 |
| 规格: | 10 mg | 产品价格: | ¥1670.0 |
| 规格: | 1 mL | 产品价格: | ¥1490.0 |
Product Introduction
Bioactivity
英文名:SCH772984
描述:SCH 772984 is a potent inhibitor of ERK1/ERK2 (IC50: 4/1 nM) and has only weak inhibitory for other 300 tested kinases.

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文献和实验疟原虫 Malaria Parasites(Plasmodium)
in one massGametocyte distorted by parasitecrescent or sausage shape; chromatin in a single mass (macrogametocyte) or diffuse (microgametocyte); dark pigment massP. vivax Ring normal to 11/4 X, round; occasionally fine Schüffner's dots; multiple infection
Dopamine Receptor Binding and Quantitative Autoradiographic Study
and extensively used to characterize the classical dopamine receptor subtypes. These radioligands include the D1 -selective ligands [3 H]SCH 23390 and [125 I]SCH 23982. D2 receptor-selective ligands include the antagonists [3 H]spiperone, [3 H]YM 09151-2, and [125
Fluorescence Correlation Spectroscopy (FCS)-Based Characterisation of Aptamer Ligand Interaction
target and its corresponding RNA aptamer selected via systematic evolution of ligands by exponential enrichment (SELEX) (Sch�rer, et al. (2001) Biol. Chem . 382 , 47948). Here, an FCS titration experiment is described in detail, where the binding
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