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. 2024 May 15;26:13. doi: 10.1186/s12575-024-00239-0

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© The Author(s) 2024

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/. 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. 6 — Validation of MUC13 expression levels in PMP. A Protein expression levels of MUC13 in soft mucin (SM – green bars) and hard mucin (HM – blue bars) [low (LG-PMP; n = 4) and high-grade (HG-PMP; n = 4)] compared to control tissues (n = 4; no tumoral appendix) evaluated by Western Blot. The arbitrary densitometric unit (ADU) for each protein was normalised by the Total Protein Normalisation (TPN) value. B Cohort validation of MUC13 by ELISA quantification SM and HM samples [low (LG-PMP) and high-grade (HG-PMP)] compared to control tissues (n = 16) (number of PMP samples analysed is indicated in the bars of the graph). One-way ANOVA analysis was performed for multiple comparisons (LG and HG-PMP vs Control). * p < 0.05 and *** p < 0.001