Method and special chemical luminous immunoassay kit for detecting clenbuterol
A chemiluminescence immunization and kit technology, applied in microorganism-based methods, biological tests, immunoglobulins, etc., can solve problems such as harm to public health, severe side effects of clenbuterol, residues in livestock and poultry products, etc., and achieve preservation. The effect of good stability and stability, high sensitivity and high specificity
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Embodiment 1
[0039] Embodiment 1, preparation and detection method of chemiluminescent immunoassay kit
[0040] 1. The chemiluminescent immunoassay kit includes:
[0041] (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 the clenbuterol hapten Conjugates with ovalbumin.
[0042] (2) Horseradish peroxidase-labeled goat anti-mouse anti-antibody working solution:
[0043] Dilute horseradish peroxidase-labeled goat anti-mouse anti-antibody with diluent, the dilution ratio is 1:2000;
[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) Cle...
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 0.1 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 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.
[0107] The experiment was repeated three times, and...
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