Fowl adenovirus strain, inactivated vaccine and preparation method
A technology of avian adenovirus and inactivated vaccine, which is applied in the field of bioengineering to achieve the effects of high safety, high protection rate against virus and rapid immune response
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0039] Embodiment 1 uses chicken embryo kidney cell (CEK cell) to prepare poultry adenovirus inactivated vaccine
[0040] The formula of the cell growth solution is: M199 solution with a volume percentage of 90%, 10% newborn bovine serum, and adjust the pH value to 7.2;
[0041] The formula of the cell maintenance solution is: M199 solution with a volume percentage of 98%, 2% newborn bovine serum, 2.4mmol / L arginine, and adjust the pH value to 7.4;
[0042] a. Preparation of CEK cells: Take 17-day-old SPF chicken embryos, take out the kidneys in a sterile environment, place them in an appropriate amount of trypsin solution, and digest them at 37°C. After the digestion is complete, take the supernatant and add an appropriate amount of serum to stop the digestion, centrifuge at 1500rpm for 10min, discard the supernatant, resuspend the cell pellet with cell growth medium and dilute to a final concentration of 1×10 cells. 6 Cells / ml, cultured at 37°C for 72 hours, the cells grow ...
Embodiment 2
[0053] Embodiment 2 uses chicken embryo fibroblast cell line (DF1 cell) to prepare poultry adenovirus inactivated vaccine
[0054] The formula of growth medium for cells is: DMEM / F12 solution with a volume percentage of 92%, 8% newborn bovine serum, and adjust the pH value to 7.2;
[0055] The formula of the cell maintenance solution is: 97% DMEM / F12 solution by volume, 3% newborn bovine serum, 2.2mmol / L arginine, and adjust the pH value to 7.3;
[0056] a. Cell culture:
[0057] The DF1 seed cells were removed from the liquid nitrogen and melted in a 37°C water bath, and revived with cell growth medium (DMEM / F12 medium) for culture. After 3 days of culture, the number of cells was 4.0×10 7.0 Cells / ml, and passaged according to 1:3, cultured at 37°C for 2 days;
[0058] b. Virus inoculation: avian adenovirus by 10 3.0 ELD 50 Inoculate DF1 cells per 0.1ml, add cell maintenance solution (DMEM / F12 medium), and continue culturing at 37°C;
[0059] c. Harvesting venom: When th...
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