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On the orders of magnitude of epigenic dynamics and monoclonal antibody production

dc.contributor.authorLee, Gyun Minen_US
dc.contributor.authorPalsson, Bernhard Ø.en_US
dc.contributor.authorSavinell, J. M.en_US
dc.date.accessioned2006-09-11T19:25:08Z
dc.date.available2006-09-11T19:25:08Z
dc.date.issued1989-09en_US
dc.identifier.citationSavinell, J. M.; Lee, G. M.; Palsson, B. O.; (1989). "On the orders of magnitude of epigenic dynamics and monoclonal antibody production." Bioprocess Engineering 4(5): 231-234. <http://hdl.handle.net/2027.42/47810>en_US
dc.identifier.issn0178-515Xen_US
dc.identifier.issn1615-7605en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/47810
dc.description.abstractThe hybridoma cell's maximum capacity for monoclonal antibody ( MAb ) production is estimated to be 2300–8000 MAb molecules/cell/s, using measured rates of transcription and translation, and the limitations imposed by the size of the polymerase molecule and the ribosome. Nearly all the production rates reported in the literature fall into or below this range of production rates. Data from batch cultures of hybridomas demonstrate a constant specific rate of MAb production until the time integral of the viable cell concentration reaches about 10 8 cells · h/cm 3 . At this point, some essential nutrients from the standard media are depleted, causing MAb production to decline.en_US
dc.format.extent385959 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherIndustrial Chemistry/Chemical Engineeringen_US
dc.subject.otherWaste Management/Waste Technologyen_US
dc.subject.otherFood Scienceen_US
dc.subject.otherChemistryen_US
dc.subject.otherBiotechnologyen_US
dc.subject.otherWaste Water Technology / Water Pollution Control / Water Management / Aquatic Pollutionen_US
dc.titleOn the orders of magnitude of epigenic dynamics and monoclonal antibody productionen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelBiomedical Engineeringen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemical Engineering, University of Michigan, Herbert H. Dow Building, 48109, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumDepartment of Chemical Engineering, University of Michigan, Herbert H. Dow Building, 48109, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumDepartment of Chemical Engineering, University of Michigan, Herbert H. Dow Building, 48109, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/47810/1/449_2004_Article_BF00369177.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00369177en_US
dc.identifier.sourceBioprocess Engineeringen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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