Method for detecting ractopamine and chemiluminescence immunoassay kit special for same
A chemiluminescence immunity, ractopamine technology, applied in chemiluminescence/bioluminescence, microorganism-based methods, immunoglobulins, etc., can solve the problems of ractopamine toxicity, public health, tachycardia, etc. The effect of good performance and stability, low cost and high accuracy
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Embodiment 1
[0040] Embodiment 1, preparation and detection method of chemiluminescent immunoassay kit
[0041] 1. The chemiluminescent immunoassay kit includes:
[0042] (1) It is obtained by dissolving the coating original in the coating buffer, wherein the concentration of the coating original in the coating original solution is 0.08 μg / mL; the coating original is the coupling of ractopamine hapten and ovalbumin things.
[0043] (2) Horseradish peroxidase-labeled goat anti-mouse anti-antibody working solution: obtained by diluting horseradish peroxidase-labeled goat anti-mouse anti-antibody with diluent, the dilution ratio is 1:1000;
[0044] 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.
[0045] Horseradish peroxidase-labeled goat anti-mouse anti-antibody was purchased from Jackson ImmunoResearch Laboratories Inc. catalog number 115-035-003.
[0046](3) Ractopamine ...
Embodiment 2
[0092] Embodiment 2, test kit sensitivity, accuracy and shelf life test
[0093] 1. Kit sensitivity experiment
[0094] 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.
[0095] Table 1 Statistical table of zero standard measurement results μg / L
[0096]
[0097] It can be seen from Table 1 that the minimum detection limit of the kit is 0.1 μg / L.
[0098] 2. Standard product precision test:
[0099] 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 1 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.
[0100] The experiment was repeated three times, and...
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