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超急速凍結保存法を用いたマウス初期胚の生存性に関する検討
http://hdl.handle.net/10191/40061
http://hdl.handle.net/10191/4006187cd7a2b-ec88-4e60-a580-db5c7ce1b31a
名前 / ファイル | ライセンス | アクション |
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106(10)_990-996.pdf (1.4 MB)
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Item type | 紀要論文 / Departmental Bulletin Paper(1) | |||||
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公開日 | 2016-03-25 | |||||
タイトル | ||||||
タイトル | 超急速凍結保存法を用いたマウス初期胚の生存性に関する検討 | |||||
タイトル | ||||||
言語 | en | |||||
タイトル | 超急速凍結保存法を用いたマウス初期胚の生存性に関する検討 | |||||
言語 | ||||||
言語 | jpn | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Cryopreservation | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | mouse preembryo | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | ultrarapid freezing | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Dimethyl sulfoxide (DMSO) | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | 凍結保存 | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | マウス初期胚 | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | 超急速凍結法 | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | ジメチルスルホキシド | |||||
資源タイプ | ||||||
資源 | http://purl.org/coar/resource_type/c_6501 | |||||
タイプ | departmental bulletin paper | |||||
その他のタイトル | ||||||
その他のタイトル | Effects on the Survival of mouse preembryos cryopreserved by Ultrarapid method of freezing | |||||
著者 |
七里, 和良
× 七里, 和良 |
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著者別名 | ||||||
識別子 | 127722 | |||||
識別子Scheme | WEKO | |||||
姓名 | Shichiri, Kazuyoshi | |||||
抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | The usefulness of ultrarapid freezing of mouse preembryo was investigated in comparison with conventional rapid freezing. In the present experiments, 2-cell mouse embryos were frozen under some conditions in an attempt to optimize their survival and viability in vitro. The experiments showed that embryos exposed briefly (2 to 8 minutes) to relatively high concentrations of dimethyl sulfoxide (2 to 3.5 M) and 025 M sucrose survived and developed when they were plunged directly into liquid nitrogen and thawed in a 37℃ waterbath and removed by one step dilution. DMSO was observed to be a better cryoprotectant than Propandiol (PROH) for ultrarapid freezing. Mouse preembryos were cooled in a biological freezer using 1.5 M PROH as cryoprotectant. Thawing was done at room temperature and PROH was removed by multistep dilutions. The rate of survival and development to blastocyst of zygotes by rapid, programmed freezing using PROH was 85.7% and 45.5%, and that of 2-cell stages was 76.8% and 69.8%, respectively, Similar results were achieved by ultrarapid freezing using DMSO, i. e, the rate of survival and development to blastocyst was 89.0% and 59.2% concerning zygotes and 79.1% and 64.1% concerning 2-cell stages, respectively. In conclusion, ultrarapid freezing was considered to be as effective as conventional rapid freezing, as evaluated by their subsequent development in vitro. | |||||
書誌情報 |
新潟医学会雑誌 en : 新潟医学会雑誌 巻 106, 号 10, p. 990-996, 発行日 1992-10 |
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出版者 | ||||||
出版者 | 新潟医学会 | |||||
ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 00290440 | |||||
書誌レコードID | ||||||
収録物識別子タイプ | NCID | |||||
収録物識別子 | AN00182415 | |||||
著者版フラグ | ||||||
値 | publisher |