化合物L-779450 T1953
品牌 | 厂商性质 | 产地 | 货期 |
---|---|---|---|
TargetMol | 生产商 | 美国 | 现货 |
性能特点
生化试剂,可用于动物细胞实验
规格 | CAS号 | 价格 | 操作 |
---|---|---|---|
5 mg | 303727-31-3 | ¥538.00 | 询底价 |
25 mg | 303727-31-3 | ¥1,830.00 | 询底价 |
100 mg | 303727-31-3 | ¥4,570.00 | 询底价 |
1 mL | 303727-31-3 | ¥593.00 | 询底价 |
10 mg | 303727-31-3 | ¥872.00 | 询底价 |
2 mg | 303727-31-3 | ¥329.00 | 询底价 |
1 mg | 303727-31-3 | ¥233.00 | 询底价 |
50 mg | 303727-31-3 | ¥2,890.00 | 询底价 |
Product Introduction
Bioactivity
英文名: L-779450
描述: L-779450 是一种有效的 ATP 竞争性 Raf 激酶抑制剂,IC50为 10 nM,Kd 为 2.4 nM。
激酶实验: Akt kinases assay: Akt kinases are assayed by a GSK-derived biotinylated peptide substrate. The extent of peptide phosphorylation is determined by Homogeneous Time Resolved Fluorescence (HTRF) using a lanthanide chelate (Lance)-coupled monoclonal antibody specific for the phosphopeptide in combination with a streptavidin-linked allophycocyanin (SA-APC) fluorophore which will bind to the biotin moiety on the peptide. When the Lance and APC are in proximity, a non-radiative energy transfer takes place from the Lance to the APC, followed by emission of light from APC at 655 nm. Working Solution: 100X protease inhibitor cocktail (PIC): 1 mg/mL benzamidine, 0.5 mg/mL pepstatin, 0.5 mg/mL leupeptin, 0.5 mg/mL aprotinin; 10X assay buffer: 500 mM HEPES, pH7.5, 1% PEG, 16.6 mM EDTA, 1 mM EGTA, 1% BSA, 20 mM 9-glycerol phosphate; Quench buffer 50 mM HEPES pH 7.3, 16.6 mM EDTA, 0.1% BSA, 0.1% Triton X-100, 0.17 nM labeled monoclonal antibody, 0.0067 mg/mL SA-APC; ATP/MgCl2 working solution: 1X Assay buffer, 1 mM DTT, 1X PIC, 5% glycerol, active Akt; Peptide working solution: 1X Assay buffer, 1 mM DTT, 1X PIC, 5% glycerol, 2 TM GSK biotinylated peptide. The reaction is assembled by adding 16 μL of ATP/MgCl2 working solution to the appropriate wells. MK-2206 or vehicle (1.0 μL) is added followed by 10 μL of peptide working solution. The reaction is started by adding 13 μL of the enzyme working solution and mixing. The reaction is allowed to proceed for 50 min and then stopped by the addition of 60 μL HTRF quench buffer. The stopped reactions are incubated at room temperature for at least 30 min and then read in the instrument.
存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: DMSO : 60 mg/mL (172.51 mM)
关键字: Autophagy | Raf kinases | Inhibitor | L779450 | Raf | inhibit | L-779450
相关产品: Raf inhibitor 1 dihydrochloride | LY3009120 | K-Ras(G12C) Inhibitor 6 | Dabrafenib | Regorafenib | OSI-930 | BMS-214662 | Griffipavixanthone | Sulindac sulfide | GDC-0879
相关库: Anti-Liver Cancer Compound Library | Anti-Cancer Compound Library | Glutamine Metabolism Compound Library | Bioactive Compounds Library Max | Inhibitor Library | Kinase Inhibitor Library | Anti-Obesity Compound Library | Apoptosis Compound Library | Autophagy Compound Library | Anti-Pancreatic Cancer Compound Library
化合物L-779450 T1953信息由TargetMol中国为您提供,如您想了解更多关于化合物L-779450 T1953报价、型号、参数等信息,欢迎来电或留言咨询。
注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途