“…Experiments with adherent MDCK cells (ECACC 84121903) and virus infections were performed in six-or 24-well plates. Culture and infection conditions were as described previously (Genzel et al, 2004). Stocks of influenza viruses PR8-NIBSC, PR8-RKI and WSN33 (a gift from Georg Kochs, University of Freiberg, Germany) were prepared in MDCK cells.…”
“…Experiments with adherent MDCK cells (ECACC 84121903) and virus infections were performed in six-or 24-well plates. Culture and infection conditions were as described previously (Genzel et al, 2004). Stocks of influenza viruses PR8-NIBSC, PR8-RKI and WSN33 (a gift from Georg Kochs, University of Freiberg, Germany) were prepared in MDCK cells.…”
“…MDCK cells were grown in roller bottles (Greiner, Esslingen, Germany, 850 cm 2 ) containing 250 mL cell growth medium (Sigma-Aldrich, Germany) for inoculum preparation. The detailed procedure is described elsewhere [17].…”
Section: Preculture In Roller Bottle and Large-scale Microcarrier Culmentioning
“…To address this issue, , current strategies include both simple and straightforward processes of fresh medium addition 12 and medium exchanging, and the relatively complex processes like fedbatch and perfusion. [13][14][15][16][17][18][19] In particular, one reported approach utilizes an alternating tangential flow (ATF) system. 18 With eight successful high cell-density ATF perfusion runs for the production of H1N1 virus, it was demonstrated that cell-specific virus yields could be kept constant and cell-specific infectious virus titers were even higher than those of batch cultures (Fig.…”
Section: Current Strategies To Overcome Nutritional Limitationmentioning
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