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Please use this identifier to cite or link to this item: http://scholars.ntou.edu.tw/handle/123456789/14523
DC FieldValueLanguage
dc.contributor.author趙乃賢en_US
dc.contributor.author劉富光en_US
dc.contributor.author黃家富en_US
dc.contributor.author楊志斌en_US
dc.contributor.author廖一久en_US
dc.date.accessioned2020-12-11T06:36:33Z-
dc.date.available2020-12-11T06:36:33Z-
dc.date.issued1993-
dc.identifier.urihttp://ntour.ntou.edu.tw:8080/ir/handle/987654321/44899-
dc.identifier.urihttp://scholars.ntou.edu.tw/handle/123456789/14523-
dc.description.abstract鯉魚 (Cyprinus carpio) 經由各種方式(如冷擊、高水壓、化學處理)誘發之後 ,必需經由染色體套數或 DNA 含量和對照組之比對來確認其三倍體率。本實驗室採用 的方法有一、染色體圖法 (Karyotyping method);二、銀染法(Silver staining method);三、粒度分析儀法(Coulter counter method);四、流式細胞儀法 (Flow cytometer method)。前三種方法本實驗室已陸續引進使用並不斷改進中,目前則嘗試 使用流式細胞儀作鑑定的工作。此期間不僅從結果分析來推論各種三倍體誘發方法的可 行性及其成效,而且和曾經採用之其他方法比較優缺點。 流式細胞儀分析法經多方測試,確知其特點為直接測知和 DNA 專用螢光染劑結合 之細胞核染色體內之 DNA 含量,而且藉助自動分析之功能,能正確且快速判讀染色體 倍數性,值得提供經常且大量測試魚類多倍體之用。有關誘發之結果顯示以 1℃ 冷擊 處理在不同組得到 66.6、80.4、86.2 及 86.4% 之三倍體鯉魚,而高水壓和高鈣高pH 化學處理組三倍體率則偏低,甚或為零。en_US
dc.language.isozhen_US
dc.publisher水產研究en_US
dc.title以流式細胞儀判讀人為誘發鯉魚三倍體之探討en_US
dc.typejournal articleen_US
dc.relation.journalvolume1en_US
dc.relation.journalissue2en_US
dc.relation.pagespp.39-54en_US
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.cerifentitytypePublications-
item.languageiso639-1zh-
item.fulltextno fulltext-
item.grantfulltextnone-
item.openairetypejournal article-
crisitem.author.deptCenter of Excellence for the Oceans-
crisitem.author.deptNational Taiwan Ocean University,NTOU-
crisitem.author.parentorgNational Taiwan Ocean University,NTOU-
Appears in Collections:海洋中心
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