PVX Yunnan isolate TAS-ELISA test kit and its preparing method
A detection kit and the technology of the kit are applied in the field of enzymology or biological devices, and can solve the problems of no TAS-ELISA detection kit, no report on the large-scale detection of plant viruses, etc.
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[0060] The collection and detection process is as follows: the diseased plant samples are collected in the field, and detected by electron microscope and standard antibody to contain a large amount of PVX, and only contain the virus. The extraction buffer was 0.2M PBS (pH7.4, containing 0.5% mercaptoethanol, 0.01M EDTA).
[0061] The purification process is:
[0062] Cut 50g of diseased leaves into pieces, add 100mL of extraction buffer, fully homogenize with an electric mixer, filter with double gauze, add 30% chloroform to the filtrate, stir at 4°C for 30min, centrifuge at 3000g for 10min, and collect the supernatant;
[0063] Add 8% PEG, 0.1M NaCl to the supernatant, dissolve and place at 4°C for 4h or overnight; centrifuge at 10000rpm, 4°C, 20min, take the precipitate, suspend it with 0.05M citric acid buffer (pH7.4), centrifuge at 10000rpm, 4°C, 10min, a precipitate was obtained;
[0064] Suspend the precipitate with 0.01M PBS (pH7.4), centrifuge at 10000rpm, 4°C, 10min...
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