HIGH DENSITY CULTIVATION OF GENETICALLY-ENGINEERED CHO CELL LINES WITH MICROCARRIER CULTURE SYSTEMS
中国医学科学杂志(英文版)1994年第2期
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HIGH DENSITY CULTIVATION OF GENETICALLY-ENGINEERED CHO CELL LINES WITH MICROCARRIER CULTURE SYSTEMS
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中图分类号:R363
纸质出版日期:1994
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[1]肖成祖,黄子才,刘凤云,郭志霞,高丽华.HIGH DENSITY CULTIVATION OF GENETICALLY-ENGINEERED CHO CELL LINES WITH MICROCARRIER CULTURE SYSTEMS[J].Chinese Medical Sciences Journal,1994(02):71-74.
HIGH DENSITY CULTIVATION OF GENETICALLY-ENGINEERED CHO CELL LINES WITH MICROCARRIER CULTURE SYSTEMS[J]. Chinese medical sciences journal, 1994, (2).
[1]肖成祖,黄子才,刘凤云,郭志霞,高丽华.HIGH DENSITY CULTIVATION OF GENETICALLY-ENGINEERED CHO CELL LINES WITH MICROCARRIER CULTURE SYSTEMS[J].Chinese Medical Sciences Journal,1994(02):71-74.DOI:
HIGH DENSITY CULTIVATION OF GENETICALLY-ENGINEERED CHO CELL LINES WITH MICROCARRIER CULTURE SYSTEMS[J]. Chinese medical sciences journal, 1994, (2).DOI:
HIGH DENSITY CULTIVATION OF GENETICALLY-ENGINEERED CHO CELL LINES WITH MICROCARRIER CULTURE SYSTEMS
were cultivated with the MC- 1 microcarrier culture system. The cell density could be enhanced by increasing the concentration of microcarrier. At a microcarrier concentration of 10 mg/ml. the cell density could reach 4 to 5 × 106 cells/ml. It was shown that these cell lines would spontaneously release from the microcarrier to attach to and proliferate on fresh microcarriers. We were thus able to scale up cultivation using a simple method. i. e. by adding fresh microcarriers and medium directly into the culture system to about 2
4 or 8 times the original volume. Using a perfusion culture system. we have successfully cultivated CLF-8B2 cells in a 2 L bioreactor for several weeks at medium perfusion rates of 0. 5 to 3working volumes. Prourokinase was stably secreted.