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. 2020 Oct 6;11:5010. doi: 10.1038/s41467-020-18852-4

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© The Author(s) 2020

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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Fig. 8 — Equal quantities of total SDS-soluble proteins from wild type, git-1(ok1848), ced-10(n3246), and pak-1(ok448), were resolved on a gel, blotted to the membrane and reacted with anti-PIX-1, and as a loading control with anti-histone H3. After normalization to the amount of histone H3, the levels of PIX-1 in the mutants were compared to the level of PIX-1 in wild type. Representative immunoblot results are shown below the graph. N = 4 independent western blot reactions from each strain; means and standard error of the means are shown; git-1 and pak-1 mutants show statistically different levels from wild-type based on a two-sided student’s t-test at p ≤ 0.0001 (indicated by ****). Images of the entire western blots are provided in the Source Data Files.