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. 2017 Jul 24;8:106. doi: 10.1038/s41467-017-00127-0

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© The Author(s) 2017

Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 4 — Remodeling of proteins involved in calcium signaling pathways in the PKP2-cKO mouse. a Representative western blots (left) and average densitometry (right; n = 6 for all groups) measured from control (CTL) and PKP2-cKO (KO) ventricular lysates. *p < 0.05; **p < 0.01 (Student’s t-test). b Immunofluorescence staining for Casq2 (green) and α-actinin (red) in control and PKP2-cKO ventricular sections collected at 21 dpi. Scale bar = 20 µm. Bottom panel: quantification of Casq2 intensity in PKP2-cKO vs. control samples. Analysis from 54 images, obtained from four hearts, both for PKP2cKo and control. ***p < 0.001 vs. control. c Immunofluorescence staining for Ankyrin B (green) and α-actinin (red) in control and PKP2-cKO heart sections at 21 dpi. Scale bar, 20 µm. Right panel: profile expression intensity of AnkB and α-actinin in PKP2-cKO and control hearts