Method for simultaneous detection of zearalenone and fumonisins
A technology of zearalenone and fumonisins, which is applied in the directions of measuring devices, instruments, scientific instruments, etc., can solve the problems of not being able to detect two toxins at the same time, affecting the detection of mycotoxins, uneconomical and environmental protection, etc. The effect of grassroots promotion and application, fast detection speed and short time required
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[0031] , Antigen preparation
[0032] (1) Preparation of zearalenone immune antigen
[0033] Take 0.33ml (3mg / ml) ZEN, mix it in 1.2ml pyridine, add 2mg O-carboxymethylhydroxylamine, stir and react at room temperature for 24h; after drying the solution in vacuum, add 4ml distilled water and dissolve it, adjust the pH to 8.0; The unreacted ZEN was removed by extraction with benzene (3 ml benzene, extracted 3 times in total), the benzene phase was removed and the water phase was retained. Adjust the pH of the aqueous phase to 3.0, extract with ethyl acetate (10ml ethyl acetate, a total of 4 extractions), extract the ester phase, and discard the aqueous phase. The ester phase was filtered with anhydrous sodium sulfate and dried. The dried crystals were dissolved in 0.5ml of dioxane treated with basic alumina; 20mg of BSA was weighed and dissolved in 0.7ml of 0.05mol / L (pH7.2) PBS; after that, the two solutions were dissolved in 4 Mix slowly at ℃ to obtain solution a; disso...
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