Preparation method of test strip for rapidly detecting chlorothalonil residues in grains
A technology of chlorothalonil and test strips, applied in the field of detection
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Embodiment 1
[0017] (1) The method for preparing fluorescent probes by coupling europium nanomaterials with monoclonal antibodies is as follows: take 800 μL of 0.2moL / L borate buffer solution in a 2mL centrifuge tube, add 200 μL of polystyrene fluorescent microsphere latex, and vortex Mix well; place the centrifuge tube in a digitally controlled high-power ultrasonic instrument for 12 minutes to disperse the latex material evenly in the solution; add 40 μL of 15 mg / mL EDC aqueous solution, vortex at room temperature for 10 minutes; then 14000r / min, 10℃ Centrifuge at high speed for 10 min under the conditions, discard the supernatant to remove excess EDC, redissolve the precipitate with 1mL borate buffer, repeat the sonication step; add a certain amount of antibody aqueous solution, vortex and mix, and transfer to a shaker shaker at room temperature After 12 hours, fully couple the antibody with the microsphere material; repeat the centrifugation step, discard the supernatant to remove the u...
Embodiment 2
[0023] (1) The method for preparing fluorescent probes by coupling europium nanomaterials with monoclonal antibodies is as follows: take 800 μL 0.2moL / L borate buffer solution in a 2 mL centrifuge tube, add 200 μL polystyrene fluorescent microsphere latex, and vortex to mix Uniformly; place the centrifuge tube in a digitally controlled high-power ultrasonic instrument for 10 minutes to disperse the latex material evenly in the solution; add 40 μL of 15 mg / mL EDC aqueous solution, vortex at room temperature for 15 minutes; then 14000r / min, 10℃ Centrifuge at high speed for 10min, discard the supernatant to remove excess EDC, redissolve the precipitate with 1mL boric acid buffer, repeat the sonication step; add a certain amount of antibody aqueous solution, vortex and mix, and transfer to a shaker shaker at room temperature for 12h , to fully couple the antibody to the microsphere material; repeat the centrifugation step, discard the supernatant to remove the uncoupled antibody, r...
Embodiment 3
[0029] (1) The method for preparing fluorescent probes by coupling europium nanomaterials with monoclonal antibodies is as follows: take 800 μL of 0.2moL / L borate buffer solution in a 2mL centrifuge tube, add 200 μL of polystyrene fluorescent microsphere latex, and vortex Mix well; place the centrifuge tube in a digitally controlled high-power ultrasonic instrument for 15 minutes to disperse the latex material evenly in the solution; add 40 μL of 15 mg / mL EDC aqueous solution, vortex at room temperature for 18 minutes; then 14000r / min, 10℃ Centrifuge at high speed for 10 min under the conditions, discard the supernatant to remove excess EDC, redissolve the precipitate with 1mL borate buffer, repeat the sonication step; add a certain amount of antibody aqueous solution, vortex and mix, and transfer to a shaker shaker at room temperature After 12 hours, fully couple the antibody with the microsphere material; repeat the centrifugation step, discard the supernatant to remove the u...
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