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Cell growth on microcarriers: comparison of proliferation on and recovery from various substrates

dc.contributor.authorVarani, Jamesen_US
dc.contributor.authorBendelow, Matthew J.en_US
dc.contributor.authorChun, John H.en_US
dc.contributor.authorHillegas, William A.en_US
dc.date.accessioned2006-04-07T19:39:19Z
dc.date.available2006-04-07T19:39:19Z
dc.date.issued1986en_US
dc.identifier.citationVarani, James, Bendelow, Matthew J., Chun, John H., Hillegas, William A. (1986)."Cell growth on microcarriers: comparison of proliferation on and recovery from various substrates." Journal of Biological Standardization 14(4): 331-336. <http://hdl.handle.net/2027.42/26400>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B7G7R-4BNF5XS-6P/2/5159279d2d07c087bad078f64b1e75caen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/26400
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=3558416&dopt=citationen_US
dc.description.abstractThree commercially-important types of cell were grown on four different microcarrier substrates. The cells, which included normal human diploid fibroblasts (MRC-5), primary chick embryo cells and Madin-Darby bovine kidney cells (MDBK), were compared with regard to proliferation on the substrates and with regard to recovery of viable cells from the same substrates. The substrates used included glass-coated microcarriers (Biosil), collagen microcarriers (Ventregel), DEAE-dextran microcarriers (Cytodex I) and collagen-linked DEAE-dextran microcarriers (Cytodex III). The established cell line (MDBK) grew well on all of the substrates and a high percentage of viable cells could be harvested from each substrate. The MRC-5 cells also grew well on all four substrates but high recovery rates were achieved only with cells grown on the glass-coated microcarriers or collagen microcarriers. In contrast, the primary chick embryo cells grew well only on the glass microcarriers and the recovery rate of cells harvested from this substrate was high. In some industrial operations, the re-utilization of cells after removal from the substrate is necessary. In these situations the appropriate choice of microcarriers for the cultivation of the cells may be critical.en_US
dc.format.extent406651 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleCell growth on microcarriers: comparison of proliferation on and recovery from various substratesen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelPharmacy and Pharmacologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pathology, The University of Michigan Medical School, Ann Arbor, Michigan 48109, USAen_US
dc.contributor.affiliationumDepartment of Pathology, The University of Michigan Medical School, Ann Arbor, Michigan 48109, USAen_US
dc.contributor.affiliationotherDivision of Viral Vaccines, Connaught Laboratories, Ltd., Willowdale M2R 3T4, Ontario, Canadaen_US
dc.contributor.affiliationotherSoloHill Engineering, Inc., Ann Arbor, Michigan 48109, USAen_US
dc.identifier.pmid3558416en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/26400/1/0000487.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0092-1157(86)90020-Xen_US
dc.identifier.sourceJournal of Biological Standardizationen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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