Antigens and polyclonal antibodies for differentiating Tilletia tritici and Tilletia tritici
A technology of Tilletia dwarf and Tilletia glabris, applied in peptide preparation methods, chemical instruments and methods, anti-animal/human immunoglobulin, etc., can solve difficult to distinguish, destructive hazards of wheat production, Complex procedures and other issues, to achieve the effect of simple operation
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Embodiment 1
[0037] Example 1. Preparation of polyclonal antibodies for identifying TCK and TFL
[0038] Reagents and solutions:
[0039] Freund's complete adjuvant, Freund's incomplete adjuvant (Beijing Qinbang Biotechnology Co., Ltd.), phosphate buffer (PBS, 0.02M, pH7.2), coating solution (phosphate buffer, 0.05M, pH7 .4), reaction diluent (PBS1, 0.03M, pH7.4+0.05% Tween 20), washing working solution (dilute the 20× concentrated washing solution with deionized water at a volume ratio of 1:19); blocking solution (Add 0.05% BSA in 0.02mol / L PBS1), substrate chromogenic solution: composed of A liquid and B liquid, A liquid is hydrogen peroxide, B liquid is tetramethylbenzidine; stop solution (2mol / L H 2 SO 4 ), enzyme-labeled secondary antibody (Beijing Qinbang Biotechnology Co., Ltd.).
[0040] Tilletia triticum suspension 1*10 5 Spore / ml
[0041] Main equipment:
[0042]Vacuum freeze dryer, electric thermostat incubator, ProteinA / G column, electrophoresis tank, electrophoresis appa...
Embodiment 2
[0088] Embodiment 2. Adopt antibody of the present invention to distinguish Tilletia tritici and Tilletia tritici
[0089] The spores of T. tritici and T. tritici spores preserved in the laboratory were used as antigens to react with the purified antibody obtained in Example 1 respectively, and the antibody blocking solution was used as a negative control. The steps were as follows:
[0090] a, wrapping plate: the polypeptide coating in embodiment 1 is diluted mass volume ratio 1:1000 times with antigen diluent originally, and Tilletia tritici is diluted 200 times with antigen diluent, add enzyme label plate respectively, every hole 100ul, incubate at 37°C for 2 hours, wash the plate once, and pat dry;
[0091] b. Blocking: Add blocking solution for blocking, 150ul per well, incubate at 37°C for 2 hours, discard the solution, pat dry, and set aside;
[0092] c, adding antibody: the polyclonal antibody prepared in Example 1 is diluted to a certain concentration with antibody d...
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