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Growth of three established cell lines on glass microcarriers

dc.contributor.authorCarani, Jamesen_US
dc.contributor.authorDame, Michael K.en_US
dc.contributor.authorBeals, Theodore F.en_US
dc.contributor.authorWass, John A.en_US
dc.date.accessioned2006-04-28T16:29:37Z
dc.date.available2006-04-28T16:29:37Z
dc.date.issued1983-05en_US
dc.identifier.citationCarani, James; Dame, Michael; Beals, Ted F.; Wass, John A. (1983)."Growth of three established cell lines on glass microcarriers." Biotechnology and Bioengineering 25(5): 1359-1372. <http://hdl.handle.net/2027.42/37890>en_US
dc.identifier.issn0006-3592en_US
dc.identifier.issn1097-0290en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/37890
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=18548765&dopt=citationen_US
dc.description.abstractThree established cell lines were examined for growth on a newly developed microcarrier which consists of glass beads. The cells were simultaneously exmined for growth on commercially available microcarriers made from DEAE-dextran and from plastic. Cell yields on the glass microcarriers were comparble to the cell yields on the commercially available products. Cells grown on the glass microcarriers were easily separated from the substratum by trypsinization (as were the cells grown on the plastic substratum) while the cells grown on the DEAE-dextran particles were much more trypsin resistant. After removal of cells from the glass microcarriers, the cells reattached and spread out in plastic flasks as readily as cells harvested from monolayer. Scanning electron microscopy revealed dramatic differences in the appearence of the cell grown on the glass microcarriers and cells grown on the DEAE-dextran microcarriers. On the glass microcarriers, cells attached to the substratum through lond, slender filopodia while on the DEAE-dextran microcarriers, the entire edge of the cell appeared to be in contact with the substratum. This dissimilarity in attachment could underly the difference in sensitivity to trypsin-mediated detachment. Finally, the glass microcarriers were washed after being used once and retested for their ability to support cell growth a second time. Nearly identical results were obtained with the reprocessed beads as with previously unused ones.en_US
dc.format.extent853678 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherChemistryen_US
dc.subject.otherBiochemistry and Biotechnologyen_US
dc.titleGrowth of three established cell lines on glass microcarriersen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbsecondlevelEcology and Evolutionary Biologyen_US
dc.subject.hlbsecondlevelMathematicsen_US
dc.subject.hlbsecondlevelNatural Resources and Environmenten_US
dc.subject.hlbsecondlevelStatistics and Numeric Dataen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelSocial Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pathology, The University of Michigan Medical School, Ann Arbor, Michigan 48109 ; Department of Pathology, The University of Michigan Medical School, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationumDepartment of Pathology, The University of Michigan Medical School, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationumDepartment of Pathology, The University of Michigan Medical School, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationumDepartment of Pathology, The University of Michigan Medical School, Ann Arbor, Michigan 48109en_US
dc.identifier.pmid18548765en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/37890/1/260250515_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/bit.260250515en_US
dc.identifier.sourceBiotechnology and Bioengineeringen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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