Myclobutanil colloidal gold test strip and preparation method and application thereof
A technology for detecting test paper and myclobutanil, which is applied in the field of myclobutanil colloidal gold detection test strip and its preparation, can solve the problems of many interfering substances, being easily affected by impurity interference, long detection time, etc., and achieving accuracy and precision High degree of accuracy, easy to promote and use, and the effect of short detection time
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[0026] The preparation method of the myclobutanazole colloidal gold detection test strip of the present invention comprises the preparation of myclobutanazole antigen, the preparation of myclobutanazole polyclonal antibody, the preparation of colloidal gold, the preparation of myclobutanazole polyclonal antibody-colloidal gold marker, the preparation of sheep antibody Rabbit anti-antibody preparation, colloidal gold detection test strip assembly steps, specifically include:
[0027] A. Myclobutanil antigen preparation:
[0028] The synthesis route of myclobutanazole antigen is as follows:
[0029]
[0030] A. Myclobutanil antigen preparation:
[0031] A1. Weigh 1.45 g of myclobutanil and dissolve it in 2 mL of dichloromethane, then add 2.5 mL of 30wt% hydrogen peroxide aqueous solution, 0.34 g of tetrabutylammonium bisulfate and 1.9 mL of 20wt% sodium hydroxide aqueous solution, and react The mixture was stirred at room temperature at 1000-2000 rpm for 24 h, then diluted ...
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[0055] Example: Preparation of Myclobutanil Colloidal Gold Test Strips
[0056] 1. Preparation of myclobutanazole antigen, that is, the preparation of myclobutanazole immune antigen and myclobutanazole-coated antigen:
[0057] 1.1. Weigh 1.45 g of myclobutanil and dissolve it in 2 mL of dichloromethane, then add 2.5 mL of 30wt% hydrogen peroxide aqueous solution, 0.34 g of tetrabutylammonium bisulfate and 1.9 mL of 20wt% sodium hydroxide aqueous solution, and react The mixture was stirred at room temperature at 1000-2000 rpm for 24 h, then diluted with 5 mL of dichloromethane, separated by TLC, washed with 5×2 mL of brine, and the precipitated white solid I was collected.
[0058] 1.2. Dissolve 0.7 g of white solid I in 0.96 mL of concentrated sulfuric acid, and heat to 70 °C, then add 0.3 mL of 0.7 g / mL sodium nitrite solution, continue to heat up to 105 °C and stir for 3 h, then cool to At room temperature, add 0.5mL of 0.01moL / L sodium hydroxide solution, extract 3 times w...
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