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α-Amanitin
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
α-Amanitin图片
CAS NO:23109-05-9
包装与价格:
包装价格(元)
100 μg电议
500 μg电议
1mg电议
2mg电议
5mg电议
10mg电议
50mg电议

产品名称
alpha-鹅膏覃碱
α-Amatoxin
产品介绍
α-Amanitin 是几种致命毒蘑菇的主要毒素,通过抑制RNA 聚合酶 II (RNA-polymerase II) 发挥其毒性作用。
生物活性

α-Amanitin is the principal toxin of several deadly poisonous mushrooms, exerting its toxic function by inhibitingRNA-polymerase II.

IC50& Target

Traditional Cytotoxic Agents

 

体外研究
(In Vitro)

α-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 LD50of 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]. α-Amanitin dramatically decreases the expression of gap junctional genes (Gja1, Gja4 and Gjc1) and FSHr and LHr in cumulus cells[4].

体内研究
(In Vivo)

The intravenous LD50dose 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 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 (Hsp90b1, Irx4, 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].

分子量

918.97

性状

Solid

Formula

C39H54N10O14S

CAS 号

23109-05-9

中文名称

alpha-鹅膏毒素;alpha-鹅膏毒肽;alpha-鹅膏菌素;alpha-鹅膏覃碱

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

-20°C, protect from light

*该产品在溶液状态不稳定,建议您现用现配,即刻使用。

溶解性数据
In Vitro: 

H2O : 100 mg/mL(108.82 mM;Need ultrasonic)

DMSO : 50 mg/mL(54.41 mM;ultrasonic and warming and heat to 60℃)

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM1.0882 mL5.4409 mL10.8817 mL
5 mM0.2176 mL1.0882 mL2.1763 mL
10 mM0.1088 mL0.5441 mL1.0882 mL
*

请根据产品在不同溶剂中的溶解度,选择合适的溶剂配制储备液;该产品在溶液状态不稳定,建议您现用现配,即刻使用

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂:

——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

  • 1.

    请依序添加每种溶剂: PBS

    Solubility: 25 mg/mL (27.20 mM); Clear solution; Need ultrasonic and warming and heat to 60℃

*以上所有助溶剂都可在本网站选购。