Nano-colloidal gold marker immunization measurement method for testing carbofuran pesticide
A nano-colloid and immunoassay technology, which is applied in the direction of measuring devices, biological testing, material inspection products, etc., to achieve the effects of stable sensitivity, simple reaction and operation, and fast detection speed
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Embodiment 1
[0021] The immune hapten was synthesized by thermal method. Take 100g of furanol and add it to a 250ml three-necked flask, then add 19g of catalyst trimethylbenzyl ammonium chloride, heat to 95°C with electric stirring, and pass phosgene into it at a certain flow rate for 2 hours. Precipitation occurred, and structural characterization was carried out by sampling, gas spectrometry, and mass spectrometry. Then weigh 4.6g of 6-aminocaproic acid and dissolve it in 6.4ml of 4mol / L NaOH solution, add it to a 250ml flask, cool to 4°C in an ice bath, weigh 7.18g of benzofuryl chloroformate and dissolve it in 20ml of dioxane In the three-neck flask, under the condition of stirring, it was added into a three-necked flask five times at intervals of 10 minutes and reacted for two hours. The pH value was adjusted to 4.0, extracted three times with ethyl acetate, and a white precipitate was precipitated, washed with water and dried.
Embodiment 2
[0026]The immune hapten was synthesized by thermal method. Take 100g of furanol and add it to a 250ml three-necked flask, then add 19g of catalyst trimethylbenzyl ammonium chloride, heat to 95°C with electric stirring, and pass phosgene into it at a certain flow rate for 2 hours. Precipitation occurred, and structural characterization was carried out by sampling, gas spectrometry, and mass spectrometry. Then weigh 4.6g of 6-aminocaproic acid and dissolve it in 6.4ml of 4mol / L NaOH solution, add it to a 250ml flask, cool to 4°C in an ice bath, weigh 7.18g of benzofuryl chloroformate and dissolve it in 20ml of dioxane In the three-neck flask, under the condition of stirring, it was added into a three-necked flask five times at intervals of 10 minutes and reacted for two hours. The pH value was adjusted to 4.0, extracted three times with ethyl acetate, and a white precipitate was precipitated, washed with water and dried.
[0027] Then, the immune antigen and the coating antigen ...
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