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. 2022 Jan 19;12:1024. doi: 10.1038/s41598-022-04971-z

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© The Author(s) 2022

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 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/.

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Confirmation of selected protein expression changes in the regression experiment using the porcine model of dietary NAFLD development. Representative Western blots (extracted from original, Supplemental Fig. S2) of proteins and quantification of their expressions normalized to the ACTIN (40 kDa) as loading control (A). Parallel reaction monitoring detection of proteotypic peptides and quantification of detectable proteins in targeted proteomics (B). Representative chromatograms of proteotypic peptide (VAVNDAHLLQYNHR for LGALS3). PSMs mascot values were divided by their protein molecular weight and the number of detected proteins of each sample. Data are expressed as mean ± SD for each group. Statistical analyses were carried out using Mann–Whitney U test. *p < 0.05. Representative micrographs of immunohistochemical localization of LGALS3 in the liver (C). Positive signals of immune labelling are shown in brown. Bar denotes 50 μm.