Amplification method of porcine epidemic diarrhea virus S-gene epitope
A porcine epidemic diarrhea and epitope technology, applied in the direction of microbial-based methods, genetic engineering, plant genetic improvement, etc., can solve problems such as unspecified S genes
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Embodiment 1
[0080] A method for amplifying the porcine epidemic diarrhea virus S gene epitope, comprising the following steps:
[0081] 1) Extraction of viral RNA: centrifuge the water sample feces of pigs at 12000rpm for 5 minutes, take the supernatant or cell culture medium at -20°C for 2-3 times, and then use Ta Ka Ra mini BEST viral RNA / DNA extraction kit Ver .4.0 (DV819A) Extract viral RNA;
[0082] Use TaKaRa mini BEST viral RNA / DNA extraction kit Ver.4.0 (DV819A) to extract viral RNA in sequence as follows:
[0083] ①Put 200μl of disease material treatment solution or frozen-thawed cell culture solution into a 1.5ml centrifuge tube, add 200μl of Solution A, shake vigorously and mix well, and place at room temperature for 5 minutes;
[0084] ② Add 75 μl of Solution B, mix well, and centrifuge at 12,000 rpm for 5 minutes;
[0085] ③ Transfer the supernatant to a new Collection Tube (2ml, provided in the kit), add 250μl of isopropanol (containing 1% glacial acetic acid), and mix up ...
Embodiment 2
[0142] The 15th generation of viral RNA extracted in Example 1 and cultured on Vero cells was amplified according to the same steps as in Example 1 to amplify a 782bp target fragment (comprising the neutralization antigenic epitope sequence between 1495bp-1914bp of the S gene) , the determined sequence is SEQ ID NO:6.
Embodiment 3
[0144] The 30th generation of viral RNA extracted in Example 1 and cultured on Vero cells was amplified according to the same steps as in Example 1 to amplify a 782bp target fragment (comprising the neutralization antigenic epitope sequence between 1495bp-1914bp of the S gene) , the determined sequence is SEQ ID NO:7.
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