Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Patrik O. Michel"'
Autor:
Clara J. Douet, David L. Hacker, Stéphanie Tissot, Lucia Baldi, Florian M. Wurm, Patrik O. Michel, Sarah Grezet
Publikováno v:
Processes
Volume 1
Issue 1
Pages 3-11
Processes, Vol 1, Iss 1, Pp 3-11 (2013)
Volume 1
Issue 1
Pages 3-11
Processes, Vol 1, Iss 1, Pp 3-11 (2013)
We investigated the cultivation of bacterial, mammalian and insect cells in an orbitally-shaken 250-mL disposable tube that incorporates a helical track (HT) on its inside wall. The mass transfer coefficient of oxygen (kLa) was 200%–400% higher in
Autor:
Stéphanie Tissot, Maria De Jesus, Lucia Baldi, Patrik O. Michel, David L. Hacker, Florian M. Wurm
Publikováno v:
New Biotechnology
The aim of this study was to gain a better understanding of orbitally shaken bioreactors (OSRs) operated without controllers for pH and dissolved oxygen (DO) concentration. We used cylindrical OSRs with working volumes ranging from 250mL to 200L to d
Autor:
Lea Hedman, Patrik O. Michel, Christian Oker-Blom, Jouni Toivola, Maria Söderlund-Venermo, Anna R. Mäkelä, Klaus Hedman, Eila Korhonen
Publikováno v:
Journal of Virological Methods. 152:1-5
Human parvovirus B19 is an autonomously replicating human pathogen with a specific tropism for human erythroid progenitor cells. There is an interest in producing empty nucleocapsids of B19 as they can be used as tools in molecular biology and diagno
Autor:
Jouni Toivola, Matti Vuento, Leona Gilbert, Varpu Marjomäki, Klaus Hedman, Tomi Lahtinen, Christian Oker-Blom, Patrik O. Michel
Publikováno v:
Biological Chemistry. 385:87-93
Fluorescence correlation spectroscopy (FCS) was used in monitoring human parvovirus B19 virus-like particle (VLP) antibody complexes from acute phase and pastimmunity serum samples. The Oregon Green 488-labeled VLPs gave an average diffusion coeffici
Publikováno v:
Michel, P, Torkkeli, T, Karp, M & Oker-Blom, C 2001, ' Expression and purification of polyhistidine-tagged firefly luciferase in insect cells : A potential alternative for process scale-up ', Journal of Biotechnology, vol. 85, no. 1, pp. 49-56 . https://doi.org/10.1016/S0168-1656(00)00377-1
The coleopteran firefly, Photinus pyralis, luciferase was produced in lepidopteran Trichoplusia ni insect cells using a baculovirus expression vector. The recombinant protein was equipped with a polyhistidine affinity tag at the carboxyl terminus and
Publikováno v:
BMC Proceedings, Vol 5, Iss Suppl 8, p P37 (2011)
BMC Proceedings
BMC Proceedings
BackgroundSf-9 cells, derived fromSpodoptera frugiperda,arewidely used for recombinant protein production usingthe baculovirus expression vector system (BEVS). How-ever, this results in a productive viral infection and celllysis. Therefore, a non-lyt
Publikováno v:
Biotechnology letters. 33(5)
Here we present the TubeSpin bioreactor 50 (TubeSpins) as a simple and disposable culture system for Sf-9 insect cells in suspension. Sf-9 cells had substantially better growth in TubeSpins than in spinner flasks. After inoculation with 10(6) cells/m
Autor:
Birgit I, Schenk, Patrik O, Michel, Gisela, Enders, Niklas, Thilo, Martina, Radtke, Christian, Oker-Blom, Dieter, Franke
Publikováno v:
Clinical laboratory. 53(3-4)
Diagnosis of acute primary Epstein-Barr Virus (EBV) infection is predominantly performed by serology. Detection of specific antibodies to defined EBV antigens is considered state of the art. Antibodies to EBNA-1 are not produced early in primary infe
Autor:
Matti Vuento, Daniel J. White, Jouni Toivola, Patrik O. Michel, Leona Gilbert, Christian Oker-Blom
Publikováno v:
Comptes rendus biologies. 328(12)
Analysis of the breakdown products of engineered viral particles can give useful information on the particle structure. We used various methods to breakdown both a recombinant enveloped virus and virus-like particles (VLPs) from two non-enveloped vir
Properties of baculovirus particles displaying GFP analyzed by fluorescence correlation spectroscopy
Publikováno v:
Biological chemistry. 383(12)
Recombinant baculovirus particles displaying green fluorescent protein (GFP) fused to the major envelope glycoprotein gp64 of the Autographa californica multicapsid nucleopolyhedrovirus (AcMNPV) were characterized by fluorescence correlation spectros