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. 2019 Nov 12;19:22. doi: 10.1186/s12861-019-0203-y

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© The Author(s). 2019

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 — Optical sectioning using structured-illumination microscopy. a Schematic drawing of a S10b-follicle placed between an object slide and a cover slip. The focal plane of tangential optical sections to analyse basal microfilaments (bMF) and microtubules (MT) in the FCE is shown as dashed red line. b Overlay of a differential interference-contrast (DIC) image and a fluorescent-phalloidin image showing the analysed area of bMF in the FCE (and, in addition, in the NC) in S10b