Monoclonal antibody for O, O-dimethoxythiophosphate pesticides
A technology of dimethoxythiophosphoric acid and monoclonal antibody, which is applied in the fields of genetic engineering, plant gene improvement, biochemical equipment and methods, and achieves the effects of low professional technical level, expanded detection range, and large analysis capacity
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Embodiment 1
[0052] Detect O in the tap water sample of embodiment 1, O-dimethoxy phosphorothioate (taking methyl parathion as an example) pesticide residue
[0053] Main conditions of ELISA reaction system
[0054] "3-Methyl 4-nitrophenyl-O-butyric acid-ovalbumin conjugate" coating 2.5μg / ml was added to each well of the microanalysis plate in 50μl, and the monoclonal antibody was diluted 32 times as the working concentration , 1% gelatin as a blocker, the methanol content in the antigen-antibody reaction solution phosphate-Tween buffer is 5%, the pH value is 7.4, the ionic strength is 0.15mol / L, and each hole in the microanalysis plate is 50 μl.
[0055] Sample preparation for testing
[0056] Tap water sample: Measure 1L of tap water, add 2mg of methyl parathion standard standard net weight, and prepare a 2ppm liquid sample.
[0057] The above samples were detected by ELISA detection method, and the operation was as follows:
[0058] (1) Coated
[0059] "3-Methyl 4-nitrophenyl-O-buty...
Embodiment 2
[0079] Detect O in the peach fruit sample of embodiment 2, O-dimethoxy phosphorothioate (taking methyl parathion as an example) residual
[0080] The main conditions of the ELISA reaction system are the same as in Example 1.
[0081] Sample preparation for testing
[0082] Peach fruit sample: Weigh 10 g of chopped peach fruit, add 0.01 mg net weight of methyl parathion, and prepare a solid sample of 1 ppm.
[0083] The above samples were detected by ELISA detection method, and the operation was as follows:
[0084] Steps (1), (2) are the same as in Example 1.
[0085] (3) Add antibody and the mixture of antibody and sample to be tested
[0086] Weigh 0.1 g of the sample to be tested, soak it in 0.2 ml of methanol for about 1 hour, take 100 μL and add it to 400 μL of phosphate buffer containing 0.5% Tween 20 to prepare the test solution, and dilute the cell culture supernatant 16 times with the test solution The test solution and the phosphate buffer containing 0.5% Tween 2...
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