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- CAS号:
331244-89-4
- 规格:
1mg/1mLx10mM(inDMSO)/5mg/10mg/25mg/50mg/100mg/200mg
| 规格: | 1mg | 产品价格: | ¥138.0 |
|---|---|---|---|
| 规格: | 1mLx10mM(inDMSO) | 产品价格: | ¥325.0 |
| 规格: | 5mg | 产品价格: | ¥278.0 |
| 规格: | 10mg | 产品价格: | ¥423.0 |
| 规格: | 25mg | 产品价格: | ¥840.0 |
| 规格: | 50mg | 产品价格: | ¥1264.0 |
| 规格: | 100mg | 产品价格: | ¥1904.0 |
| 规格: | 200mg | 产品价格: | ¥2848.0 |
Product Introduction
Bioactivity
| 名称 | BAM7 |
| 描述 | BAM 7 is a direct and specific activator of proapoptotic Bax (EC50: 3.3 μM). |
| 细胞实验 | MEFs (2.5 × 103 cells per well) are seeded in 96-well opaque plates for 18-24 h and then incubated with serial dilutions of BAM7, ANA-BAM16 or vehicle (0.15% (v/v) DMSO) in DMEM at 37 °C in a final volume of 100 μL. Cell viability is assayed at 24 h by addition of CellTiter-Glo reagent according to the manufacturer's protocol, and luminescence is measured using a SpectraMax M5 microplate reader. Viability assays are performed in at least triplicate, and the data are normalized to vehicle-treated control wells.(Only for Reference) |
| 激酶实验 | Fluorescence polarization binding assays: Direct binding curves are first generated by incubating FITC-BIM SAHB (50 nM) with serial dilutions of fulllength BAX, BCL-XLΔC, MCL-1ΔNΔC, BFL-1/A1ΔC or BAKΔC and fluorescence polarization measured at 20 minutes on a SpectraMax M5 microplate reader. For competition assays, a serial dilution of small molecule or acetylated BIM SAHB (Ac-BIM SAHB) is combined with FITC-BIM SAHB (50 nM), followed by the addition of recombinant protein at ~EC75 concentration, as determined by the direct binding assay (BAX, BAKΔC: 500 nM; BCL-XLΔC, MCL-1ΔNΔC, BFL-1/A1ΔC: 200 nM). Fluorescence polarization is measured at 20 minutes and IC50 values calculated by nonlinear regression analysis of competitive binding curves using Prism software. |
| 体内活性 | 体外实验中,BAM7触发BAX-介导的孔形成,BAX低聚化及BAX-依赖的细胞死亡。通过触发细胞内BAX激活,BAM7可选择性诱导BAX-介导的细胞凋亡。BAM7只对含BAX的细胞系有杀灭效果,产生BAX-介导的细胞凋亡的生化和形态特征。BAM7可与BAX的N-末端的BH3结构结合沟直接结合。BAM7与BAX直接在表面相互作用,经BIM BH3螺旋触发BAX激活。BAM7剂量和时间性地触发BAX从单体到低聚物的转换。 |
| 存储条件 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
| 溶解度 | DMSO : 4.1 mg/mL (10.11 mM), Sonication is recommended. |
| 关键字 | Inhibitor | inhibit | Bcl-2 Family | Bax | BAM-7 | BAM7 | BAM 7 |
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| 相关库 | Bioactive Compound Library | Anti-Cancer Compound Library | Bioactive Compounds Library Max | Mitochondria-Targeted Compound Library | Apoptosis Compound Library | Anti-Aging Compound Library | Hematonosis Compound Library | Cuproptosis Compound Library | Target-Focused Phenotypic Screening Library | PPI Inhibitor Library |
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文献和实验网络 第十九章 杂环化合物和生物碱 杂环化合物在自然界分布很广,其数量几乎占已知有机化合物的三分之一,用途也很多。许多重要的物质如叶绿素、血红素、核酸以及临床应用的一些有显著疗效的天然药物和合成药物等,都含有杂环化合物的结构。生物碱多是中草药的有效成分,绝大多数是含氮的杂环化合物。本章内容与医学关系密切,具有重要意义。
分子中具有高能键的化合物。在生物体内主要有上式(Ⅰ)和(Ⅱ)两种结构的高能化合物。其作用为贮藏能量(例如 ATP、肌酸磷酸)和作为产生 ATP源的中间代谢产物(例如磷酸烯醇丙酮酸)以及合成反应的中间物质(例如酰基辅酶 A),在蛋白质的结构( conformation)变化周期的第一阶段上(例如钠钾 ATP酶的羧基磷酸中间体)也具有重要作用。多数高等化合物具有磷酸基,但也有例外。
由不同种元素组成的纯净物叫做化合物。化合物一般有固定的组成。化合物的组成一般可用化学式表示。化合物具有确定的物理性质和化学性质,不同于其组成元素的性质。化合物中的元素不能用简单的机械方法或物理方法分开,而必须用化学方法才能分离。
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