Application of rainbow trout ifn-γ2 in preparation of anti-ihn virus products
A virus and the technology in the sequence list, applied in the direction of antiviral agents, medical preparations containing active ingredients, recombinant DNA technology, etc., can solve problems such as recessive infection, high mortality of fry or juvenile fish, etc.
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Embodiment 1
[0026] Example 1. Obtaining of rainbow trout IFN-γ2 gene and its recombinant vector for expression
[0027] 1. Cloning of the target gene
[0028] The rainbow trout (Oncorhynchus mykiss, kept and bred in the laboratory, is a conventional rainbow trout species) was killed, the head kidney and spleen were aseptically stripped on ice quickly, and an appropriate amount of MEM medium containing 10% FBS was added, and the inner column of the syringe was rolled and passed through Filter through a 70 μm nylon mesh (product of Fisher Scientific), stimulate with 5 μg / mL phytohemagglutinin, and extract total RNA using Promega’s RNA extraction kit. According to the instructions of M-MLV reverse transcriptase, use primer Oligo(dT) 18 was reverse transcribed to obtain the first strand of cDNA.
[0029] Referring to the published rainbow trout IFN-γ2 sequence (Genbank: FM864345.1), design upstream and downstream primers for amplifying rtIFN-γ2, upstream primer: 5'-ATC GGATCC GCTCAGTACACAT...
Embodiment 2
[0040] Embodiment 2, application of rainbow trout IFN-γ2 gene
[0041] 1. Protein expression and expression pattern analysis
[0042]The recombinant strain DH5α / pET32a-rtIFN-γ2 was cultured in 5mL LB medium containing 100μg / mLAMP at 37°C overnight with shaking at 220rpm. The next day, the overnight culture was inoculated in 100mL LB medium at a ratio of 1:100, cultured with shaking at 220rpm until the OD value reached 0.6-0.8, and the expression was induced by adding 1mMIPTG. After 4h, the cells were collected by centrifugation at 4000rpm at 4°C.
[0043] The bacteria were resuspended in PBS with 1 / 10 of the initial medium volume, and divided into supernatant and precipitate after ultrasonic lysis and crushing. SDS-PAGE was used to analyze the existing form of the target protein.
[0044] The result is as figure 2 As shown, M is the protein molecular mass standard; 1 is before the induction of the expression strain; 2 is after the induction of the expression strain; 3 is th...
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