Method and special quantum dot fluorescent immunoassay kit for detecting quinolone compounds
A technology of quinolones and fluorescent immunity, applied in the direction of microorganism-based methods, chemical instruments and methods, biochemical equipment and methods, etc., can solve problems such as human health hazards and ecological environment pollution, and achieve low cost, high sensitivity, and sample The effect of simple pre-processing
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Embodiment 1
[0038] Embodiment 1, preparation and detection method of quantum dot fluorescence immunoassay kit
[0039] 1. Quantum dot fluorescence immunoassay kit includes:
[0040] (1) Original coating solution: obtained by dissolving the original coating in the coating buffer, wherein the concentration of the original coating in the original coating solution is 0.08 μg / mL; the original coating is quinolone compound hapten and Bovine serum albumin conjugate;
[0041] (2) Quantum dot-labeled goat anti-mouse anti-antibody working solution:
[0042] It is obtained by diluting quantum dot-labeled goat anti-mouse anti-antibody with diluent, and the dilution ratio is 1:500;
[0043] The diluent is obtained by mixing 50mL bovine serum albumin and 950mL phosphate buffer; the concentration of the phosphate buffer is 0.02M, and the pH value is 7.4.
[0044] Goat anti-mouse anti-antibody was purchased from Beijing Boaosen, the product catalog number is bs-0295G.
[0045] (3) norfloxacin standard ...
Embodiment 2
[0099] Embodiment 2, test kit sensitivity, accuracy and shelf life test
[0100] 1. Kit sensitivity experiment
[0101] The zero standard solution (that is, the diluent is pH7.4, 0.05M phosphate buffer) was tested 20 times, and the average value of the measurement results plus 3 times the standard deviation was used as the minimum detection limit of the kit.
[0102] Table 1 Statistical table of zero standard measurement results μg / L
[0103]
[0104] It can be seen from Table 1 that the minimum detection limit of the kit is 0.5 μg / L.
[0105] 2. Standard product precision test:
[0106] From the three batches of kits described in Example 1 (batch 01, batch 02, and batch 03), 10 kits were extracted from each batch, and the luminous intensity value of the 4.5 μg / L standard solution was measured to calculate the coefficient of variation. The detection method is consistent with that described in Experiment 3 in Example 1.
[0107] The experiment was repeated three times, a...
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