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Productivity, apoptosis, and infection dynamics of influenza A/PR/8 strains and A/PR/8-based reassortants
Authors:Isken B  Genzel Y  Reichl U
Institution:Max Planck Institute for Dynamics of Complex Technical Systems, Bioprocess Engineering, Sandtorstrasse 1, 39106 Magdeburg, Germany. isken@mpi-magdeburg.mpg.de
Abstract:In cell culture-based influenza vaccine production significant efforts are directed towards virus seed optimization for maximum yields. Typically, high growth reassortants (HGR) containing backbones of six gene segments of e.g. influenza A/PR/8, are generated from wild type strains. Often, however, HA and TCID50 titres obtained do not meet expectations and further optimization measures are required.
Keywords:FITC  fluorescein isothiocyanate  HA  hemagglutinin  HGR  high growth reassortant  hpi  hours post infection  MDCK  madin-darby canine kidney  MOI  multiplicity of infection  NA  neuraminidase  NIBSC  National Institute of Biological Standards and Control  NP  nucleoprotein  RKI  Robert Koch Institute  TCID50  50% tissue culture infective dose
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