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  1. 原著論文

A new method for the simple and temperature-permissive cryopreservation of mouse embryos.

https://repo.qst.go.jp/records/47303
https://repo.qst.go.jp/records/47303
b6d2ec9b-1f39-406d-8b9f-269d4beb4297
Item type 学術雑誌論文 / Journal Article(1)
公開日 2015-09-16
タイトル
タイトル A new method for the simple and temperature-permissive cryopreservation of mouse embryos.
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Mochida, Keiji

× Mochida, Keiji

WEKO 473135

Mochida, Keiji

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Hasegawa, Ayumi

× Hasegawa, Ayumi

WEKO 473136

Hasegawa, Ayumi

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Li, Ming-Wen

× Li, Ming-Wen

WEKO 473137

Li, Ming-Wen

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D., Fray Martin

× D., Fray Martin

WEKO 473138

D., Fray Martin

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Kito, Seiji

× Kito, Seiji

WEKO 473139

Kito, Seiji

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M., Vallelunga Jadine

× M., Vallelunga Jadine

WEKO 473140

M., Vallelunga Jadine

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C., Kent Lloyd K.

× C., Kent Lloyd K.

WEKO 473141

C., Kent Lloyd K.

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Yoshiki, Atsushi

× Yoshiki, Atsushi

WEKO 473142

Yoshiki, Atsushi

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Obata, Yuichi

× Obata, Yuichi

WEKO 473143

Obata, Yuichi

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Ogura, Atsuo

× Ogura, Atsuo

WEKO 473144

Ogura, Atsuo

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鬼頭 靖司

× 鬼頭 靖司

WEKO 473145

en 鬼頭 靖司

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抄録
内容記述タイプ Abstract
内容記述 Procedures for cryopreserving embryos vary considerably, each having its specific advantages and disadvantages in terms of technical feasibility, embryo survival yield, temperature permissibility and species- or strain-dependent applicability. Here we report a high osmolality vitrification (HOV) method that is advantageous in these respects. Cryopreservation by vitrification is generally very simple, but, unlike slow freezing, embryos should be kept at a supercooling temperature (below –130uC) to avoid cryodamage. We overcame this problem by using an HOV solution containing 42.5% (v/v) ethylene glycol, 17.3% (w/v) Ficoll and 1.0 M sucrose. This solution is more viscous than other cryopreservation solutions, but easy handling of embryos was assured by employing a less viscous equilibration solution before vitrification. Most (.80%) embryos cryopreserved in this solution survived at –80uC for at least 30 days. Normal mice were recovered even after intercontinental transportation in a conventional dry-ice package for 2–3 days, indicating that special containers such as dry shippers with liquid nitrogen vapor are unnecessary. The HOV solution could also be employed for long-term storage in liquid nitrogen, as with other conventional cryoprotectants. Finally, we confirmed that this new vitrification method could be applied successfully to embryos of all six strains of mice we have tested so far. Thus, our HOV method provides an efficient and reliable strategy for the routine cryopreservation of mouse embryos in animal facilities and biomedical laboratories, and for easy and cheap transportation.
書誌情報 PLoS ONE (Online only:URL:http://www.plosone.org)

巻 8, 号 1, p. 1-8, 発行日 2013-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 1932-6203
DOI
識別子タイプ DOI
関連識別子 10.1371/journal.pone.0049316
関連サイト
識別子タイプ URI
関連識別子 http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0049316
関連名称 http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0049316
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