Immunofluorescence detection method for measuring virus carried rate of vector insects
A technology for immunofluorescence detection and mediator insects, which is applied in the direction of fluorescence/phosphorescence, measuring devices, and material analysis through optical means, can solve the problems of not being suitable for large-scale sample detection, high technical requirements, and high detection costs, and achieve shortening The detection time, the result is intuitive and accurate, and the effect of short time consumption
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[0033] 1. Reagent preparation
[0034] 1) 0.01mol / L PBS: Weigh 8 g NaCl, 0.2 g KCl, 1.44 g Na 2 HPO 4 and 0.24 g KH 2 PO 4 , dissolved in 800 ml of distilled water, adjusted the pH value to 7.2 with HCl, and added distilled water to make the volume to 1L.
[0035] 2) Fixative solution: Weigh 4 g of paraformaldehyde and dissolve it in 100 ml of 0.01 mol / L PBS buffer solution, heat and stir at 50°C-60°C to dissolve, and store at 4°C.
[0036] 3) Permeate: Add 0.2 mL of TritonX-100 solution to 10 mL of 0.01 mol / L PBS buffer, stir well to dissolve, and store at 4°C.
[0037] 4) Antibody diluent: Weigh 0.3g BSA into a 15ml centrifuge tube, add 10mL of 0.01 mol / L PBS buffer, stir well to dissolve, and store at 4°C.
[0038] 5) Anti-fading solution: Measure 90 ml of glycerol and 10 mL of 0.01 mol / L PBS buffer solution, mix well, and store at 4°C.
[0039] 6) Fluorescent antibody: For southern rice black-streaked dwarf virus (SRBSDV), firstly, the IgG of the polyclonal antibod...
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