Grass carp reovirus S11 gene eukaryotic expression recombinant plasmid preparation method and application thereof in serving as nucleic acid vaccine
A technology of reovirus and recombinant plasmid, applied in the fields of genetic engineering and molecular immunology, to achieve good immunogenicity and simple preparation method
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0030] Preparation of Grass Carp Reovirus S11 Target Gene Nucleic Acid Vaccine
[0031] 1. Construction of grass carp reovirus recombinant plasmid S11-pcDNA3.1
[0032] Grass carp reovirus was isolated from a breeding pond in Xinxiang City, Henan Province. Grass carp viscera suffering from grass carp hemorrhagic disease were obtained, mixed with PBS buffer, ground and homogenized, and the homogenate was centrifuged at 8000g, and the supernatant was filtered through a filter with a pore size of 0.22µm , the filtrate was inoculated into the grass carp kidney cells (CIK) cultured in vitro, and the cells were collected after one week of culture, and the cells contained the proliferating grass carp reovirus. The total RNA of cells and viruses was extracted, and RT-PCR detection showed that the grass carp reovirus was type II grass carp reovirus. Grass carp reovirus genomic RNA was used as a template, and primers S11F: 5'-TGTGGATCCACCAATTATCGGTAAGTATGGAA-3' and primers S11R: 5'-CTG...
Embodiment 2
[0038] Application of Grass Carp Reovirus Recombinant Plasmid S11-pcDNA3.1 as Nucleic Acid Vaccine
[0039] 1. Grass carp reovirus S11 target gene nucleic acid vaccine can significantly stimulate the increase in the number of immune cells in fish
[0040] 90 healthy grass carp fry (about 20 g per fish) were randomly divided into 3 groups, 30 fish in each group, as the experimental group, the empty plasmid control group and the negative control group respectively, and each fish in the experimental group was intramuscularly injected with nucleic acid vaccine 0.5 μg / g Fish body weight, the empty plasmid control group was injected with the same amount of pcDNA-3.1 empty vector plasmid, the negative control group was injected with the same volume of PBS buffer, and raised at 25°C. On the 1st, 7th, 14th, 21st, 28th, 35th, 42nd, and 49th day after injection, 3 fish were taken from each of the 3 groups every day, and the blood was taken from the tail vein, diluted with a volume ratio ...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com