Expi293F cell culture method
A culture method and cell technology, applied in the culture process, animal cells, tissue culture, etc., can solve the problems of unfavorable mass transfer, shear rate cell damage, etc., and achieve the effect of expanding mass transfer, reducing physical damage, and high-density cells
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Embodiment 1
[0016] Example 1 Cultivation of Expi293F cells
According to the cell density 0.2 × 10 6 cells / ml The cells were inoculated into a 50-liter Qizhi bioreactor (working volume was 40L) for dynamic perfusion culture for 48 hours, and the serum-free medium to be perfused was divided into 6 strands. (The medium to be perfused was preheated Treated to 37°C), uniformly dispersed along the inner wall of the bioreactor, and perfused into the bioreactor by adhering to the wall. During the dynamic culture of perfusion, keep the culture conditions in the reactor: temperature 37°C, DO 40-60%, pH7.2 ± 0.2; The serum-free medium used in the culture process is: 24.75g / L Dynamis medium 95wt%, 200 mM glutamine 4wt%, and anti-agglomeration agent 1wt%.
[0017] The injection rate of culture solution is: in the early stage of cell growth, the injection rate of culture solution is 0.5 working volume / d, the stirring speed is 85 rpm, and in the stable phase of cell growth, the injection rate of cult...
Embodiment 2
[0019] The culture medium injection rate was: in the early stage of cell growth, the culture medium injection rate was 0.5 working volume / d, the stirring speed was 86 rpm, and the cell growth was stable, the culture medium injection rate was 1 working volume / d, and the stirring speed was 85 rpm. , the cell growth period is vigorous, the culture medium injection rate is 2 working volumes / d, and the stirring speed is 81 rpm.
Embodiment 3
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