Method for suspension culture of subculture cells and method for producing hog cholera vaccine by using subculture cells
A suspension culture and cell technology, applied in the field of medicine and biology, can solve the problems of failure to achieve full suspension culture of cells
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Embodiment 1
[0066] Embodiment 1 Utilizes genetic modification suspension culture ST cell
[0067] 1) Stable transfection of ST cells with an expression vector containing the siat7e gene;
[0068] (1) Escherichia coli DH5α competent cells were transfected with a full-length human siat7e gene expression vector (Cat.No.EX-V1581-M03, Genecopoeia). Plasmid DNA was extracted using an endotoxin-free plasmid extraction kit (QIAGEN).
[0069] (2) Day 1: transfer 5×10 5 ST cells (provided by the China Veterinary Drug Administration) were incubated in a 6-well plate, and the cells were incubated for 24 hours at about 90% confluence.
[0070] (3) On the next day, take 10 μg of plasmid DNA and dilute it in 250 μL Opti-MEM medium, mix well; 50 μL liposomes are diluted in 250 μL Opti-MEM medium, mix gently, and let stand for 15 minutes.
[0071] (4) Mix the solutions prepared above, and let stand at room temperature for 20min; replace each well of the 6-well plate described in step (2) with 2 mL of O...
Embodiment 2-4
[0084] Except that the experimental conditions were changed according to Table 1, the same operations as in Example 1 were carried out.
[0085] Table 1
[0086]
[0087]
Embodiment 5
[0088] Embodiment 5 utilizes the method for the ST cell production swine fever vaccine of large-scale culture genetic modification suspension culture
[0089] A part of the cells verified by suspension culture (ST cells, Example 1) was frozen and stored, and the other part was continued to be cultured in the cell culture flask. When the cells grow normally in cell culture flasks and their viability is greater than 90%, they are inoculated into shake flasks. Expand cultured cells in shake flasks, press 3×10 5 The cells / mL cell density were inoculated into a 650L bioreactor (Beijing Qingda Tianyi Technology Co., Ltd.), and the cell culture conditions were as follows:
[0090] Working volume: 300L
[0091] Cell culture temperature: 37°C
[0092] pH: 7.0
[0093] Dissolved oxygen: 40%;
[0094] Cell culture medium: modified MEM cell culture medium MD611 (Beijing Qingda Tianyi Technology Co., Ltd.) + 5% serum
[0095] Cultured for 4 days, when the cell density was 3×10 6 Cells...
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