A kit for detecting porcine pseudorabies antibody
A technology of porcine pseudorabies and porcine pseudorabies virus, applied in the field of kits for detecting porcine pseudorabies antibodies, can solve the problems of low specificity, prone to false positives, low sensitivity, etc., and achieves low detection cost and is not easy to be false Positive or false positive error judgment, high sensitivity effect
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Embodiment 1
[0047] The kit for detecting porcine pseudorabies antibody provided in this embodiment includes an enzyme-linked plate coated with porcine pseudorabies virus gE antigen, rabbit anti-pig IgG antibody labeled with horseradish peroxidase, rapid coating solution, and rapid blocking solution , sample diluent, TMB chromogenic solution, stop solution, 20 times concentrated washing solution, negative control, positive control.
[0048] The fast coating solution is NaOH with a concentration of 0.1 mol / L and a pH of 13; the fast blocking solution is KOH with a concentration of 0.1 mol / L and a pH of 13.
[0049] The sample dilution is obtained by adding casein and NaN in PBS at a concentration of 0.01M and a pH of 7.2 3 Prepared with casein and NaN in the sample diluent 3 The mass fractions were 1% and 0.001%, respectively.
[0050] The TMB concentration in the described TMB chromogen is 0.3g / L; The stop solution is that the concentration is 2M H 2 SO 4 Solution; Among them, TMB chro...
Embodiment 2
[0069] The present embodiment provides the method for detecting the pseudorabies antibody with the kit for detecting the pseudorabies antibody, comprising the following steps:
[0070] (1) Test sample preparation: After blood collection, centrifuge at 3000 rpm for 5 minutes, and take the supernatant to obtain serum;
[0071] (2) Equilibration: Take the kit out of the refrigerated environment and equilibrate at room temperature for 30 minutes before use;
[0072] (3) With lotion: dilute 20 times concentrated lotion with double distilled water 20 times for later use;
[0073] (4) Setting: Set wells A1-A6 in the microtiter plate, where no sample diluent is added to wells A1 and A2, 100 μL positive control serum is added to wells A3 and A4, and 100 μL negative control is added to wells A5 and A6 Serum, that is, wells A1 and A2 are blank controls, wells A3 and A4 are positive controls, and wells A5 and A6 are negative controls;
[0074] (5) Adding samples: Add 100 μL of detection...
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