Bovine viral diarrhea virus (BVDV) transgenosis Astragalus mongholicus vaccine and production method
A technology of bovine viral diarrhea and virus genes, applied in biochemical equipment and methods, antiviral agents, genetic engineering, etc., can solve problems such as low protection, poor immunogenicity of nucleic acid vaccines, unsafe use of live virus vaccines, etc. To achieve the effect of no negative effects, fast gene homozygosity, and safe use
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[0076] 1. Bovine viral diarrhea virus gene E 0 Gene acquisition
[0077] Using the bovine viral diarrhea virus genomic RNA extracted by the conventional method of extracting RNA as a template, the reverse transcription-polymerase chain reaction was used to amplify E 0Gene. The primer sequences used for the amplification are as follows: upstream: 5′-CCGGATCCACCATGGAAAACATAACACAGTGG-3′; downstream: 5′-GCGAGCTCTTAAGCGTATGCTCCAAACCACGT-3′. After the product of reverse transcription-polymerase chain reaction was subjected to agarose gel electrophoresis, the target gene E 0 See figure 1 .
[0078] 2. Bovine viral diarrhea virus gene E 0 Construction of recombinant plant expression vector
[0079] Digest the gel-purified target gene E with DNA restriction endonuclease 0 and plant expression vector DNA, ligated with T4 DNA ligase at 16°C for 16 hours, took 5 μl of the ligated product to transform competent E. Identification of endonuclease double digestion and sequence analysi...
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