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. 2024 Aug 10;11:868. doi: 10.1038/s41597-024-03697-z

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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/.

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Fig. 5 — Technical repeats for the secretome screen. Graphs to show the reproducibility of the raw data between the two replica plates for nuclear number (a) and EdU negative (EdU-) fraction (b) in MCF7 cells (p < 0.0001). Graphs to show the reproducibility of the raw data between the two replica plates for nuclear number (c) and EdU negative (EdU-) fraction (d) in hTERT-HMEC cells (p < 0.0001). Note that the data for hTERT-HMEC EdU- fraction is noisy for hTERT-HMEC cells but proteins are only called as a hit if they increased the EdU- (G0) fraction in both technical replicates.