{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Matthews JL"],"funding":["NCRR NIH HHS","NIH HHS"],"pagination":["279-290"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC5985902"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["15(3)"],"pubmed_abstract":["Sperm cryopreservation is a highly efficient method for preserving genetic resources. It extends the reproductive period of males and significantly reduces costs normally associated with maintenance of live animal colonies. However, previous zebrafish (Danio rerio) cryopreservation methods have produced variable outcomes and low post-thaw fertilization rates. To improve post-thaw fertilization rates after cryopreservation, we developed a new extender and cryoprotective medium (CPM), introduced quality assessment (QA), determined the optimal cooling rate, and improved the post-thaw in vitro fertilization process. We found that the hypertonic extender E400 preserved motility of sperm held on ice for at least 6 h. We implemented QA by measuring sperm cell densities with a NanoDrop spectrophot"],"journal":["Zebrafish"],"pubmed_title":["Changes to Extender, Cryoprotective Medium, and In Vitro Fertilization Improve Zebrafish Sperm Cryopreservation."],"pmcid":["PMC5985902"],"funding_grant_id":["R24 OD011120","R24 OD010441","R24 RR023998","P40 OD011021"],"pubmed_authors":["Yang H","Varga ZM","Carmichael C","Murphy JM","Tiersch T","Westerfield M","Matthews JL"],"additional_accession":[]},"is_claimable":false,"name":"Changes to Extender, Cryoprotective Medium, and In Vitro Fertilization Improve Zebrafish Sperm Cryopreservation.","description":"Sperm cryopreservation is a highly efficient method for preserving genetic resources. It extends the reproductive period of males and significantly reduces costs normally associated with maintenance of live animal colonies. However, previous zebrafish (Danio rerio) cryopreservation methods have produced variable outcomes and low post-thaw fertilization rates. To improve post-thaw fertilization rates after cryopreservation, we developed a new extender and cryoprotective medium (CPM), introduced quality assessment (QA), determined the optimal cooling rate, and improved the post-thaw in vitro fertilization process. We found that the hypertonic extender E400 preserved motility of sperm held on ice for at least 6 h. We implemented QA by measuring sperm cell densities with a NanoDrop spectrophot","dates":{"release":"2018-01-01T00:00:00Z","publication":"2018 Jun","modification":"2025-04-04T08:27:22.689Z","creation":"2025-04-04T08:27:22.689Z"},"accession":"S-EPMC5985902","cross_references":{"pubmed":["29369744"],"doi":["10.1089/zeb.2017.1521"]}}