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. 2019 Nov 4;9:15876. doi: 10.1038/s41598-019-52456-3

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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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Overview of the proteins identified in the C-PSCs and H-PSCs samples. (a) The numbers of proteins exclusively detected in each sample or shared between them are indicated in the diagram. Only proteins identified by at least two peptides and present in the two biological replicates were considered for analysis. (b) Volcano plot of proteins shared between C-PSCs and H-PSCs, with significant differences between samples. Proteins with a p value < 0.05 (−log₁₀ = 1.3) and a fold-change (FC) > 1.5 (log₂ = 0.5) were considered differentially abundant between H-PSC and C-PSC by both statistical and FC parameters and are represented by black dots and identified by their numbering in Table S4. Proteins without significant differences in abundance between samples according to the criteria above are shown as grey dots.