Vitrification of mouse embryos by vitroloop technique

dc.creatorVass, Nóra
dc.creatorKlambauer, Philip
dc.creatorJávor, András
dc.creatorKeresztes, Zsuzsa
dc.creatorCeh, Sándor
dc.date2009-12-21
dc.date.accessioned2021-06-28T10:57:26Z
dc.date.available2021-06-28T10:57:26Z
dc.descriptionThe objective of the study was to vitrify mouse embryos with the cryoloop technology using a new combination of vitrification mediums. Embryos were exposed to a 2- step loading of CPA, ethylene glycol and propylene glycol, before being placed on the surface of a thin filmy layer formed from the vitrification solution in a small nylon loop. After warming, the CPA was diluted out from the embryos by a 3-step procedure. Our data show that a high percentage of embryos survived (92.7%) vitrification in the mixture of EG and PG combined with cryoloop carrier and developing normally (89.1%) in vitro after thawing. 
dc.formatapplication/pdf
dc.identifierhttps://ojs.lib.unideb.hu/actaagrar/article/view/2786
dc.identifier10.34101/actaagrar/37/2786
dc.identifier.urihttp://hdl.handle.net/2437/316403
dc.languageeng
dc.publisherFaculty of Agricultural and Food Sciences and Enviromental Management of the Debrecen University, Debrecen.
dc.relationhttps://ojs.lib.unideb.hu/actaagrar/article/view/2786/2799
dc.sourceActa Agraria Debreceniensis; No. 37 (2009); 81-83
dc.source2416-1640
dc.source1587-1282
dc.subjectvitrification
dc.subjectmouse embryos
dc.subjectvitroloop
dc.titleVitrification of mouse embryos by vitroloop technique
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.typePeer-reviewed Article
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