Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Fumonisin B1 is the most abundant and toxic fumonisin and is a mycotoxin produced from Fusarium moniliforme. Fumonisin B1 is also a potent inhibitor of sphingosine N-acyltransferase (ceramide synthase) and disrupts de novo sphingolipid biosynthesis.
规格 | 价格/CNY | 货期 | 数量 | |
---|---|---|---|---|
1 mg | ¥ 1,270 | 35日内发货 | ||
5 mg | ¥ 5,670 | 35日内发货 | ||
10 mg | ¥ 9,430 | 35日内发货 |
产品描述 | Fumonisin B1 is the most abundant and toxic fumonisin and is a mycotoxin produced from Fusarium moniliforme. Fumonisin B1 is also a potent inhibitor of sphingosine N-acyltransferase (ceramide synthase) and disrupts de novo sphingolipid biosynthesis. |
体外活性 | Fumonisin B1 changes the gene expression and signal transduction pathways in monkey kidney cells. Fumonisin B1 increases the initial disruption of sphingolipid metabolism and the accumulation of sphinganine in LLC-PK1 kidney cells. Which causes DNA damage of apoptotic type in rat astrocytes [3]. |
别名 | 伏马菌素B1 |
分子量 | 721.83 |
分子式 | C34H59NO15 |
CAS No. | 116355-83-0 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Methanol: 10 mg/mL (13.85 mM), Sonication and heating are recommended.
可选溶剂 | 浓度 体积 质量 | 1 mg | 5 mg | 10 mg | 25 mg |
Methanol | 1 mM | 1.3854 mL | 6.9268 mL | 13.8537 mL | 34.6342 mL |
5 mM | 0.2771 mL | 1.3854 mL | 2.7707 mL | 6.9268 mL | |
10 mM | 0.1385 mL | 0.6927 mL | 1.3854 mL | 3.4634 mL |
对于不同动物的给药剂量换算,您也可以参考 更多...
请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法: 比如您的给药剂量是10 mg/kg,每只动物体重20 g,给药体积100 μL,一共给药动物10 只,您使用的配方为5% DMSO+30% PEG300+5% Tween 80+60% ddH2O。那么您的工作液浓度为2 mg/mL。
母液配置方法:2 mg 药物溶于 50 μL DMSO (母液浓度为 40 mg/mL), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:取 50 μL DMSO 主液,加入 300 μL PEG300, 混匀澄清,再加 50 μL Tween 80,混匀澄清,再加 600 μL ddH2O, 混匀澄清。
您可能有的问题的答案可以在抑制剂处理说明中找到,包括如何准备库存溶液,如何存储产品,以及基于细胞的分析和动物实验需要特别注意的问题。
Fumonisin B1 116355-83-0 Others 伏马菌素B1 Fumonisin B-1 Inhibitor inhibitor inhibit