| CAS: | 1227633-49-9 | |
| 分子式: | C24H23N5OS | |
| 分子量: | 429.54 | |
| 英文名称: |
| |
| 用途: | StemRegenin 1 是一种有效的芳香烃受体 (AhR) 拮抗剂,IC50 为 127 nM。 |
| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | 详情 | ||||||||||||||||||||||||||||||||||
| S860852 | MACKLIN | SetmEegenin 1 | >98% | 339元/10mg; 1159元/50mg; 1992元/100mg; | 展开 | ||||||||||||||||||||||||||||||||||
储存:-20℃ 状态:白色固体 折射率:white solid | |||||||||||||||||||||||||||||||||||||||
| S795814 | MACKLIN | SetmEegenin 1 | 10mM in DMSO | 361元/1ml; | 展开 | ||||||||||||||||||||||||||||||||||
储存:-20°C | |||||||||||||||||||||||||||||||||||||||
| 182706 | Sigma-Aldrich | AhR Antagonist II, SR1-CAS 1227633-49-10-Calbiochem | The AhR Antagonist II, SR1 controls the biological activity of AhR. This small molecule/inhibitor is primarily used for Biochemicals applications. | 2538.8元/5 MG; | 展开 | ||||||||||||||||||||||||||||||||||
产品说明 一般描述 A cell-permeable purine compound that acts as a high affinity AhR antagonist (IC50 = 127 nM against 3 nM TCDD-induced luciferase reporter activity in HepG2 cultures), but not a panel of 61 kinases. AhR expression and function knockouts by shRNAs, CH-223191 (Cat. No. 182705), or SR1 treatment all result in enhanced and sustained CD34+ population in long-term proliferating/expanding cultures of cord blood-derived HSCs (hematopoietic setem cells) in serum-free media containing Tpo (Cat. No. 605218), SCF (Cat. No. 569600), Flt3 Ligand (Cat. No. 343010), and IL-6 (Cat. No. 407652) in a reversible manner. SR1 is reactive toward human, monkey, and canine, but not rat or murine, species. 包装 5 mg in Glass bottle 警告 Toxicity: Regulatory Review (Z) 重悬 Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C. 其他说明 Boitano, A.E., et al. 2010. Science329, 1345. 法律信息 CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany 基本信息
产品性质
安全信息
| |||||||||||||||||||||||||||||||||||||||