Publication:
Comparing in Vitro Embryonic Development of Bovine Oocytes Cultured in G1.3/G2.3 Sequential Culture Media and Crlaa Medium

dc.authorscopusid23396214300
dc.authorscopusid6602400461
dc.authorscopusid24472081300
dc.authorscopusid23767133200
dc.authorscopusid55919600100
dc.authorscopusid6603553213
dc.contributor.authorÇevik, M.
dc.contributor.authorSaǧirkaya, H.
dc.contributor.authorTas Ekiz, A.
dc.contributor.authorAkkoç, T.
dc.contributor.authorBaǧiş, H.
dc.contributor.authorArat, S.
dc.date.accessioned2025-12-10T21:40:13Z
dc.date.issued2009
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Çevi̇k] Mesut, Department of Animal Reproduction and Artificial Insemination, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Saǧirkaya] Hakan, Department of Reproduction and Artificial Insemination, Bursa Uludağ Üniversitesi, Bursa, Bursa, Turkey; [Tas Ekiz] Arzu, Research Institute for Genetic Engineering and Biotechnology, Gebze, Kocaeli, Turkey; [Akkoç] Tolga, Research Institute for Genetic Engineering and Biotechnology, Gebze, Kocaeli, Turkey; [Baǧiş] Haydar, Research Institute for Genetic Engineering and Biotechnology, Gebze, Kocaeli, Turkey; [Arat] Sezen, Research Institute for Genetic Engineering and Biotechnology, Gebze, Kocaeli, Turkeyen_US
dc.description.abstractIn vitro embryo culture is an important step of in vitro production of bovine embryos. The aim of this study was to compare the in vitro development of bovine embryos in G1.3/G2.3 sequential culture media and CRlaa culture medium. Oocytes were obtained from ovaries of slaughtered cows and matured in TCM-199 medium in humidified air containing 5% CO2 at 39°C. Matured oocytes were fertilized in vitro using frozen bull sperm prepared with Percoll separation. After fertilization, the presumptive zygotes were denuded from cumulus cells and randomly allotted for 2 treatments: Culture in CR1 aa (n = 116) and Gl. 3/G2.3 (n = 125). The embryo culture was carried out in 50 μL droplets of the media that were placed in incubator containing 6% CO<inf>2</inf>, 5% O<inf>2</inf> and 89% N<inf>2</inf>. The embryos were evaluated on days 3, 5 and 7 following in vitro fertilization. The difference of cleavage rates between 2 treatments was not found significant (p>0.05). However, significant difference was observed between 2 treatments at the level of the obtaining rate of morula and blastocyst (p<0.05). The results showed that Gl.3/G2.3 sequential media significantly favoured developing of morula and blastocysts in comparison to CR1 aa medium (32.0% versus 10.40% versus 18.96 and 2.58%, respectively). © Medwell Journals, 2009.en_US
dc.identifier.endpage1189en_US
dc.identifier.issn1680-5593
dc.identifier.issue6en_US
dc.identifier.scopus2-s2.0-70350767516
dc.identifier.startpage1185en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12712/34761
dc.identifier.volume8en_US
dc.language.isoenen_US
dc.relation.ispartofJournal of Animal and Veterinary Advancesen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBovineen_US
dc.subjectCRLaaen_US
dc.subjectEmbryo Cultureen_US
dc.subjectGl.3/G2.3 Sequential Mediaen_US
dc.subjectIVFen_US
dc.titleComparing in Vitro Embryonic Development of Bovine Oocytes Cultured in G1.3/G2.3 Sequential Culture Media and Crlaa Mediumen_US
dc.typeArticleen_US
dspace.entity.typePublication

Files