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. 2023 Jul 27;30(10):1403–1413. doi: 10.1038/s41417-023-00647-6

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© The Author(s) 2023

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. 2 — A Expression of RIP1 and β-catenin in HCT116 and DLD-1 cells. Left panels: Expression of RIP1 and β-catenin. Right panels: Graph of band densities of RIP1 and β-catenin. B IP assay was performed with HCT116 and DLD-1 cells treated with or without WNT3A. C In vitro binding assay of HIS-tagged RIP1 with GST-fused β-catenin. The detailed protocol is described in the Materials and Methods. D IP analyses were performed with HCT116 and DLD-1 cells transiently transfected with Flag-Mock (pcDNA3.1) or Flag-RIP1 plasmids.