Two h y b r i d o m a cell lines were cultivated in an indirectly aerated 10-1 reactor in batch, fed-batch and continuous (perfusion) operations and in spinner flasks. The m e d i u m in the reactor was sampled either by an aseptic cross-flow filtration module integrated into a loop or by an in-situ
Continuous cultivation of hybridoma cells in cell reactor
β Scribed by Vyacheslav P. Pankratov; Yuri A. Mantzygin; Oleg S. Morenkov; Natal'ya V. Swyatukhina
- Publisher
- Springer Netherlands
- Year
- 1985
- Tongue
- English
- Weight
- 332 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0141-5492
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Cell cycle, cell size and rhodamine 123 fluorescence in cell populations of two batch cultures were analysed and quantified with a fluorescence-activated cell sorter (FACS). Two cultures derived from either exponential or stationary phase innocula were investigated in order to demonstrate the depend
## Abstract **BACKGROUND:** The production of Monoclonal antibodies (mAbs) is often performed in batch or fedβbatch operations where low cell densities and low volumetric productivities are achieved. The main bottleneck of both processes is the short operating time with productive cells at maximum