Long W J, Palombo A, Schofield T L, Emini E A
Department of Virus and Cell Biology, Merck Sharp and Dohme Research Laboratories, West Point, PA 19486.
Hybridoma. 1988 Feb;7(1):69-77. doi: 10.1089/hyb.1988.7.69.
Different cell culture media were compared for their ability to support and promote the growth of stable hybridoma cell lines derived from three commonly used parental murine myelomas. Supplemented Dulbecco's modified Eagle's media (DMEM) and RPMI 1640 media were studied. The DMEM-based media were found to support greater numbers of cells for longer time periods than were the RPMI 1640-based media. Aminopterin supplemented medium was shown to be significantly less effective in supporting hybridoma reproduction and viability than medium without aminopterin. Antibody levels were directly related to cell concentration and viability regardless of the medium used for the hybridoma culture. An optimally formulated DMEM-based medium is suggested as the medium of choice for hybridoma propagation and maintenance.
比较了不同细胞培养基支持和促进源自三种常用亲本鼠骨髓瘤的稳定杂交瘤细胞系生长的能力。研究了添加的杜尔贝科改良伊格尔培养基(DMEM)和RPMI 1640培养基。发现基于DMEM的培养基比基于RPMI 1640的培养基能在更长时间内支持更多数量的细胞。与不添加氨基蝶呤的培养基相比,添加氨基蝶呤的培养基在支持杂交瘤繁殖和活力方面明显效果较差。无论用于杂交瘤培养的培养基如何,抗体水平都与细胞浓度和活力直接相关。建议使用最佳配方的基于DMEM的培养基作为杂交瘤增殖和维持的首选培养基。