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. 2018 Mar 1;20:6. doi: 10.1186/s12575-018-0071-z

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© The Author(s). 2018

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 3 — Double fluorescence in situ hybridization of mos (red) and cyclin B1 (green) mRNAs in zebrafish ovaries. DNA is shown in blue. a-c A zebrafish ovary section showing localization of mos (a) and cyclin B1 (b) mRNAs in a fully grown oocyte. A merged image is shown in (c). The mos and cyclin B1 mRNAs were localized at the animal polar cytoplasm beneath the micropyle (m). fc, follicle cells; c, chorion. d-f High resolution imaging of the oocyte shown in a-c. The insets are enlarged views of the boxed regions. The mos and cyclin B1 mRNAs were distributed in the animal polar cytoplasm of oocyte as different granules. Bars: 50 μm in a-c, 10 μm in d-f