Spinner bottle production method of inactivated singapore grouper iridovirus (SGIV) vaccine
A technology for iridescent viruses and inactivated vaccines, applied in biochemical equipment and methods, antiviral agents, viruses/bacteriophages, etc., can solve the problems of large-scale application, high labor intensity, and high production costs, and achieve low production costs, The effect of low labor intensity and stable quality between batches
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Embodiment 1
[0020] Cell growth medium: Leibovitz's-15 (L15) medium, prepared according to the company's product instructions, and add 0.266% NaCl, 5mM HEPES to adjust the pH to 7.2~7.6. In this example, adjust the pH to 7.6, and pass through a 0.22 μm filter membrane Filter and add fetal bovine serum before use to make the volume fraction 8-10%. In this embodiment, the volume fraction is 10% fetal bovine serum.
[0021] 1. Vial culture of grouper spleen tissue cells. Take the grouper spleen tissue cells covered with a single layer, remove the original culture medium, rinse once with phosphate buffered saline (PBS), add 0.25% trypsin to digest for 1-2 minutes, then add the above cell growth solution, After blowing evenly, divide into 3 cell culture flasks for culture and expansion at 28°C.
[0022] 2. Spinner bottle culture of cells: take the above 15 75cm cells covered with monolayer grouper spleen tissue cells 2 For cell culture flasks, remove the original culture medium, rinse once wi...
Embodiment 2
[0026] Cell growth medium: Leibovitz's-15 (L15) medium, prepared according to the company's product instructions, adding 0.266% NaCl, 5mM HEPES, and adjusting the pH to 7.2~7.6. In this example, the pH was adjusted to 7.2, and passed through a 0.22 μm filter membrane Filter and add fetal bovine serum before use to make the volume fraction 8-10%. In this example, the volume fraction is 8% fetal bovine serum.
[0027] 1. Vial culture of grouper spleen tissue cells. Take the grouper spleen tissue cells covered with a single layer, remove the original culture medium, rinse once with phosphate buffered saline (PBS), add 0.25% trypsin to digest for 1-2 minutes, then add the above cell growth solution, After blowing evenly, divide into 3 cell culture flasks for culture and expansion at 28°C.
[0028] 2. Spinner bottle culture of cells: take the above 10 75cm cells covered with monolayer grouper spleen tissue cells 2For cell culture flasks, remove the original culture medium, rinse ...
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