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. 2019 Oct 10;9:14598. doi: 10.1038/s41598-019-50775-z

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© The Author(s) 2019

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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Proteome profile analysis of cochlear duct lysates with R&D Mouse Proteome Profiler Mouse Cytokine Array Panel A (a,c) and Mouse Angiogenesis Array Kit (b,d). (a,b) Representative images for Cytokine Array Panel A (B1: BLC, B7: CD54, D12: CXCL12) and Angiogenesis Array Kit (A8: TF, B4: DPPIV, B7: endostatin, B9: FGF acidic, C8: IGFBP-2, E2: osteopontin, E7: PF4, F4: serpin F1). See Supplementary Table S2 for identification of all measured proteins. (c,d) Pixel density of protein dots acquired from cochlear duct lysates. There were no significant differences in either examined factors between wild-type (WT) and PACAP-deficient (KO) mice. Mean ± SEM, Student’s t-test.