DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kim, SJ | ko |
dc.contributor.author | Han, BK | ko |
dc.contributor.author | Lee, Gyun Min | ko |
dc.date.accessioned | 2013-03-03T06:23:11Z | - |
dc.date.available | 2013-03-03T06:23:11Z | - |
dc.date.created | 2012-02-06 | - |
dc.date.created | 2012-02-06 | - |
dc.date.issued | 1995-12 | - |
dc.identifier.citation | BIOPROCESS ENGINEERING, v.12, no.1-2, pp.65 - 70 | - |
dc.identifier.issn | 0178-515X | - |
dc.identifier.uri | http://hdl.handle.net/10203/77620 | - |
dc.description.abstract | In order to test the feasibility of using calcium alginate-entrapped hybridoma cells for IgM production, HO-22-1 hybridoma cells entrapped into calcium alginate beads with varying alginate concentrations were cultivated in spinner flasks. It was observed that the IgM produced by the entrapped cells could diffuse out of the calcium alginate beads regardless of alginate concentrations tested (0.8-2.5%). Since the increase in alginate concentrations showed an adverse effect on cell growth and maximum cell concentration, the use of lower alginate concentration was desirable for higher volumetric monoclonal antibody (MAb) productivity. When the entrapped cells in 0.8% alginate beads were cultivated in repeated-fed batch mode, the reduction of serum concentration in the medium from 10% to 1% did not decrease the volumetric IgM production. Taken together, the data obtained here showed the feasibility of using calcium. alginate-entrapped hybridoma cells for IgM production. | - |
dc.language | English | - |
dc.publisher | Springer Verlag | - |
dc.subject | MONOCLONAL-ANTIBODY PRODUCTION | - |
dc.subject | ANIMAL-CELLS | - |
dc.subject | GEL BEADS | - |
dc.subject | IMMOBILIZATION | - |
dc.subject | SERUM | - |
dc.subject | DIFFUSION | - |
dc.subject | SYSTEMS | - |
dc.subject | GROWTH | - |
dc.title | FEASIBILITY STUDY ON THE USE OF CALCIUM ALGINATE-ENTRAPPED HYBRIDOMA CELLS FOR IGM PRODUCTION | - |
dc.type | Article | - |
dc.identifier.wosid | A1995QL63700010 | - |
dc.identifier.scopusid | 2-s2.0-0028821076 | - |
dc.type.rims | ART | - |
dc.citation.volume | 12 | - |
dc.citation.issue | 1-2 | - |
dc.citation.beginningpage | 65 | - |
dc.citation.endingpage | 70 | - |
dc.citation.publicationname | BIOPROCESS ENGINEERING | - |
dc.contributor.localauthor | Lee, Gyun Min | - |
dc.contributor.nonIdAuthor | Kim, SJ | - |
dc.contributor.nonIdAuthor | Han, BK | - |
dc.type.journalArticle | Article | - |
dc.subject.keywordPlus | MONOCLONAL-ANTIBODY PRODUCTION | - |
dc.subject.keywordPlus | ANIMAL-CELLS | - |
dc.subject.keywordPlus | GEL BEADS | - |
dc.subject.keywordPlus | IMMOBILIZATION | - |
dc.subject.keywordPlus | SERUM | - |
dc.subject.keywordPlus | DIFFUSION | - |
dc.subject.keywordPlus | SYSTEMS | - |
dc.subject.keywordPlus | GROWTH | - |
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