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. 2020 Jul 1;22:13. doi: 10.1186/s12575-020-00126-4

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© The Author(s) 2020

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.

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Fig. 4 — 3D visualisation of LAMA4-immunolabelled equine superficial digital flexor tendon. 3D reconstructions of an equine superficial digital flexor tendon showing longitudinal nuclear (blue; a-c) and LAMA4 (red; e-g) labelling, and with each channel overlaid to create a composite image (i-k) rotated at x = − 45°, 0°, + 45°. Transverse (xz) views of 3D reconstructions of equine SDFT (d,h,l) demonstrate signal present throughout the depth of the tissue. Interfascicular matrix (IFM) and fascicles (f) are denoted longitudinally (b) and transversely (d). Scale bars = 200 µm