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使用带有外置离心机的灌注培养容器对杂交瘤细胞进行高密度培养。

High density culture of hybridoma cells using a perfusion culture vessel with an external centrifuge.

作者信息

Tokashiki M, Arai T, Hamamoto K, Ishimaru K

机构信息

Biotechnology Research Laboratories, Tokyo Research Center, Japan.

出版信息

Cytotechnology. 1990 May;3(3):239-44. doi: 10.1007/BF00365487.

Abstract

The influence of centrifugal force on the growth of cells was examined by exposing the cells of the mouse-human hybridoma X87 line to centrifugal force (100-500 G) for ten minutes twice a day and comparing the static culture with that of unexposed cells. In this experiment, both cell proliferation and specific antibody productivity were independent of the centrifugal effect, and gave the same results as in the case of no exposure to centrifugal force. High density cultivation of the mouse-human hybridoma X87 line was obtained by a perfusion system where the cells were separated from the culture medium by continuous centrifugation. In the serum-free culture, the maximum viable cell density exceeded 10(7) cells/ml, and monoclonal antibody was stably produced for 37 days. The results in this culture were equivalent to those obtained by intermittent centrifugal cell separation from the culture medium, and separation by gravitational settlement.

摘要

通过将小鼠 - 人杂交瘤X87细胞系的细胞每天两次暴露于离心力(100 - 500G)下10分钟,并将静态培养与未暴露细胞的培养进行比较,研究了离心力对细胞生长的影响。在该实验中,细胞增殖和特异性抗体产生均与离心效应无关,并且与未暴露于离心力的情况给出相同的结果。通过灌注系统实现了小鼠 - 人杂交瘤X87细胞系的高密度培养,其中通过连续离心将细胞与培养基分离。在无血清培养中,最大活细胞密度超过10⁷个细胞/毫升,并且单克隆抗体稳定产生37天。该培养中的结果与通过从培养基中间歇性离心细胞分离以及通过重力沉降分离所获得的结果相当。

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