Application of siniperca chuatsi ISKNV (Infectious Spleen and Kidney Necrosis Virus) ORF093 protein
A technology of spleen and kidney necrosis virus, ORF093, applied in the field of genetic engineering, can solve the problem that there is no research report on ISKNVORF093 gene antiserum preparations, and achieve good immune prevention effect
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Embodiment 1
[0018] 1 Prokaryotic expression of mandarin fish ISKNV ORF093 recombinant protein in Escherichia coli
[0019] 1.1 Primers were designed according to the Infectious Spleen and Kidney Necrosis Virus (ISKNV) [NC_003494] ORF093 sequence (SEQ ID NO: 1) in GenBank, and a restriction enzyme cleavage site was introduced (underlined). The primer sequences are as follows:
[0020] P1:【5`-CG GAATTC ATGAATAAAACGC -3'] (SEQ ID NO: 3), introducing EcoRI restriction site;
[0021] P2: [5'-CGG AAGCTT TTAAACATGGCGTC -3'] (SEQ ID NO: 4), introducing a HindⅢ restriction site.
[0022] 1.2 Use the ISKNV genome of mandarin fish self-preserved in our laboratory as a template for PCR amplification. The 25 μL PCR reaction system contains: 10×buffer (including Mg2+) 2.5 μL, 4×dNTP (10 mmol / L) 0.5 μL, upstream and downstream primers (20 μmol / L) 0.5 μL each, Taq DNA polymerase (5U / μL) 0.3 μL, DNA 1.0 μL, and sterile double distilled water to make up. PCR reaction conditions: pre-denaturation at...
Embodiment 2
[0065] 1. Construction of ISKNV ORF093 eukaryotic expression vector
[0066] 1.1 Primers were designed according to the Infectious Spleen and Kidney Necrosis Virus (ISKNV) [NC_003494] ORF093 sequence (SEQ ID NO: 1) in GenBank, and a restriction enzyme cleavage site was introduced (underlined). The primer sequences are as follows:
[0067] P3: [5'-AT GGTACC A TGGTTTCGAGTGCACTGCT-3'] (SEQ ID NO: 5), introduced Kpn Ⅰ Restriction site;
[0068] P4:【5'-AT GAATTC TTAGGCCATAATGCCGCG-3'] (SEQ ID NO: 6), introducing Eco RI restriction site.
[0069]1.2 Use the pET32a-ORF 093 plasmid as a template for PCR amplification. The 25 μL PCR reaction system contains: 10×buffer (including Mg2+) 2.5 μL, 4×dNTP (10 mmol / L) 0.5 μL, upstream and downstream primers (20 μmol / L) each 0.5 μL, Taq DNA polymerase (5U / μL) 0.3 μL, DNA 1.0 μL, supplemented with sterile double distilled water. PCR reaction conditions: pre-denaturation at 94°C for 4min; denaturation at 94°C for 45S, renaturation a...
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