store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year
alpha-Amanitin is the principal toxin of poisonous mushrooms, exerting its toxic function by inhibiting RNA-polymerase II.
产品描述 | alpha-Amanitin is the principal toxin of poisonous mushrooms, exerting its toxic function by inhibiting RNA-polymerase II. |
体外活性 | Alpha-Amanitin decreases TAF15 mRNA and TAF15 protein levels in MKN45 cells and inhibits the RNAPII activity towards TAF15 mRNA [2]. alpha-Amanitin decreases cell viability by 14%, 21%, 41%, 44%, and 50% at concentrations of 100, 10, 1, 0.1, and 0.01 μg/mL, respectively. The LD50 of the alpha-Amanitin at 36 h is measured as 1 μg/mL. The total amount of protein within the cell at 24 h is significantly increased for the 1 μg/mL dose of alpha-Amanitin compared to the control [3]. Alpha-Amanitin dramatically decreases the expression of gap junctional genes and FSHr and LHR in cumulus cells [4]. |
体内活性 | The intravenous LD50 dose of alpha-Amanitin is 0.327 mg/kg body weight after intravenous injection into BALB/c mice. After 12 h of alpha-Amanitin injection in the caudal vein, the levels of WBC, RBC, and HGB decrease significantly, while those of BUN and Crea increase significantly in serum. alpha-Amanitin inhibits some genes (Irx4, Hsp90b1, etc.), whose encoded proteins regulate the RNA polymerase II activity. alpha-Amanitin down-regulates some proteins (Nmi, Trpc5, etc.) taking part in the transcription progress [1]. alpha-Amanitin has potent activity in DTC suppression. Mice injected with alpha-Amanitin (0.4?mg/kg, i.p.)-treated cells maintain their body weight, while those receiving a peritoneal injection of MKN45 cells show a constant decrease in body weight [2]. |
别名 | α-Amanitin, α-Amatoxin |
分子量 | 918.97 |
分子式 | C39H54N10O14S |
CAS No. | 23109-05-9 |
store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year
H2O: 33.33 mg/mL (36.27 mM)
可选溶剂 | 浓度 体积 质量 | 1 mg | 5 mg | 10 mg | 25 mg |
H2O | 1 mM | 1.0882 mL | 5.4409 mL | 10.8817 mL | 27.2044 mL |
5 mM | 0.2176 mL | 1.0882 mL | 2.1763 mL | 5.4409 mL | |
10 mM | 0.1088 mL | 0.5441 mL | 1.0882 mL | 2.7204 mL | |
20 mM | 0.0544 mL | 0.272 mL | 0.5441 mL | 1.3602 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。
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