{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Mustofa I"],"funding":["Universitas Airlangga"],"pagination":["e06372"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC7944040"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["7(3)"],"pubmed_abstract":["The study aimed to determine the addition of green tea extract (GTE) in extender on the quality and DNA mutation of post-thawed Kacang buck sperm. The sperm DNA mutation was observed on nicotinamide adenine dinucleotide hydride (NADH) dehydrogenase 1 (ND1) of mitochondrial Deoxyribonucleic Acid (mtDNA). A pool of 12 Kacang buck ejaculates was diluted in skim milk-egg yolk extender contained 0, 0.05, 0.10, and 0.15 mg of GTE/100 mL for T0, T1, T2, and T3 group, respectively. Each of the aliquot groups was packaged in 0.25 mL French mini straw contained 60 million alive sperm and froze according to the protocol. The ND1 mtDNA amplification of samples was carried out Polymerase Chain Reaction machine, followed by DNA sequencing using the Sanger method. Meanwhile, the phylogenetic tree was con"],"journal":["Heliyon"],"pubmed_title":["Green tea extract increases the quality and reduced DNA mutation of post-thawed Kacang buck sperm."],"pmcid":["PMC7944040"],"funding_grant_id":["360/UN3.14/PT/2020"],"pubmed_authors":["Mustofa I","Susilowati S","Wurlina W","Hernawati T","Oktanella Y"],"additional_accession":[]},"is_claimable":false,"name":"Green tea extract increases the quality and reduced DNA mutation of post-thawed Kacang buck sperm.","description":"The study aimed to determine the addition of green tea extract (GTE) in extender on the quality and DNA mutation of post-thawed Kacang buck sperm. The sperm DNA mutation was observed on nicotinamide adenine dinucleotide hydride (NADH) dehydrogenase 1 (ND1) of mitochondrial Deoxyribonucleic Acid (mtDNA). A pool of 12 Kacang buck ejaculates was diluted in skim milk-egg yolk extender contained 0, 0.05, 0.10, and 0.15 mg of GTE/100 mL for T0, T1, T2, and T3 group, respectively. Each of the aliquot groups was packaged in 0.25 mL French mini straw contained 60 million alive sperm and froze according to the protocol. The ND1 mtDNA amplification of samples was carried out Polymerase Chain Reaction machine, followed by DNA sequencing using the Sanger method. Meanwhile, the phylogenetic tree was con","dates":{"release":"2021-01-01T00:00:00Z","publication":"2021 Mar","modification":"2025-04-03T21:33:30.039Z","creation":"2022-02-10T15:46:24.875Z"},"accession":"S-EPMC7944040","cross_references":{"pubmed":["33732926"],"doi":["10.1016/j.heliyon.2021.e06372"]}}