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dc.contributor.authorSime, A. A. W.
dc.contributor.authorMcKellar, Quintin
dc.contributor.authorNolan, A. M.
dc.date.accessioned2014-01-23T14:00:31Z
dc.date.available2014-01-23T14:00:31Z
dc.date.issued1997-01
dc.identifier.citationSime , A A W , McKellar , Q & Nolan , A M 1997 , ' Method for the growth of equine airway epithelial cells in culture ' , Research in Veterinary Science , vol. 62 , no. 1 , pp. 30-33 . https://doi.org/10.1016/S0034-5288(97)90176-4
dc.identifier.issn0034-5288
dc.identifier.otherPURE: 1449163
dc.identifier.otherPURE UUID: dfffc5b5-5b41-4ab7-9236-7c9ba9bbfd2a
dc.identifier.otherScopus: 0030633669
dc.identifier.urihttp://hdl.handle.net/2299/12654
dc.description.abstractA serum-free cell culture method was developed for equine tracheal epithelial cells which allowed the growth and characterisation of the phenotypical properties of this cell type. Several variables influenced the efficacy of the attachment and growth of the isolated cells. Serum and a collagen matrix were essential components for efficient cell attachment. Once attachment had occurred, cell growth was enhanced by a serum-free medium containing bovine pituitary extract, retinoic acid, insulin, hydrocortisone, transferrin, epidermal growth factor, adrenaline and triiodothyronine. The mean time taken for the cells to grow to confluency varied from 12.6 to 28.0 days, depending on the medium used. Collagen matrix was essential to aid the proliferation of the cellsen
dc.format.extent4
dc.language.isoeng
dc.relation.ispartofResearch in Veterinary Science
dc.titleMethod for the growth of equine airway epithelial cells in cultureen
dc.contributor.institutionOffice of the Vice-Chancellor
dc.contributor.institutionVeterinary Science
dc.contributor.institutionGeography, Environment and Agriculture
dc.description.statusPeer reviewed
dcterms.dateAccepted1997-01
rioxxterms.versionofrecordhttps://doi.org/10.1016/S0034-5288(97)90176-4
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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