Method for assessing development toxicity of triazole pesticides with drosophila melanogaster
A growth and development, triazole technology, applied in the field of toxicity research, can solve problems such as ecological security and human health risks, less research on terrestrial insects, etc.
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Embodiment 1
[0042] Reagent preparation: Tebuconazole, with a purity of 97%, was purchased from Shanghai Beide Pharmaceutical Technology Co., Ltd. and dissolved in dimethyl sulfoxide. Add equal volumes of stock solutions with different concentrations to the specified concentration in the standard medium, and add equal volumes of dimethyl sulfoxide in the blank control group.
[0043] Exposure conditions: set up 2 experimental groups, 5 parallels in each group; blank control (without tebuconazole), and tebuconazole group (10 mg / L). 20 third-instar larvae were placed in each parallel experimental group for infection culture, and cultured under standard culture conditions for 7 days. The other group was cultured under standard culture conditions for 6h, 12h and 30h, then the trypan blue staining experiment was carried out. The culture medium is 77.7g cornmeal, 32.19g yeast, 10.6g agar, 0.726g CaCl 2 , 31.62g sucrose, 63.2g glucose, 2g potassium sorbate and 15ml 5% butylparaben solution. Th...
Embodiment 2
[0046] Reagent preparation: Tebuconazole, with a purity of 97%, was purchased from Shanghai Beide Pharmaceutical Technology Co., Ltd. and dissolved in dimethyl sulfoxide. Add equal volumes of stock solutions with different concentrations to the specified concentration in the standard medium, and add equal volumes of dimethyl sulfoxide in the blank control group.
[0047] Exposure conditions: set up 2 experimental groups, 5 parallels in each group; blank control (without tebuconazole), and tebuconazole group (100 mg / L). 20 third-instar larvae were placed in each parallel experimental group for infection culture, and cultured under standard culture conditions for 7 days. The other group was cultured under standard culture conditions for 6h, 12h and 30h, then the trypan blue staining experiment was carried out. The culture medium is 77.7g cornmeal, 32.19g yeast, 10.6g agar, 0.726g CaCl 2 , 31.62g sucrose, 63.2g glucose, 2g potassium sorbate and 15ml 5% butylparaben solution. T...
Embodiment 3
[0050] Reagent preparation: Tebuconazole, with a purity of 97%, was purchased from Shanghai Beide Pharmaceutical Technology Co., Ltd. and dissolved in dimethyl sulfoxide. Add equal volumes of stock solutions with different concentrations to the specified concentration in the standard medium, and add equal volumes of dimethyl sulfoxide in the blank control group.
[0051] Exposure conditions: set up 2 experimental groups, 5 parallels in each group; blank control (without tebuconazole), and tebuconazole group (250 mg / L). 20 third-instar larvae were placed in each parallel experimental group for infection culture, and cultured under standard culture conditions for 7 days. The other group was cultured under standard culture conditions for 6h, 12h and 30h, then the trypan blue staining experiment was carried out. The culture medium is 77.7g cornmeal, 32.19g yeast, 10.6g agar, 0.726g CaCl 2 , 31.62g sucrose, 63.2g glucose, 2g potassium sorbate and 15ml 5% butylparaben solution. T...
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