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. 2019 Sep 30;27(4):1355–1368. doi: 10.1038/s41418-019-0421-7

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© The Author(s) 2019

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. 5 — TXNDC12 interacts with β-catenin via the thioredoxin-like domain. a Immunoprecipitation of β-catenin with E-cadherin in the indicated HCC cells, as detected by immunoblot analysis. b E-cadherin and β-catenin expression in the indicated cells, as detected by an immunofluorescence assay. The merged images show overlays of E-cadherin (green) and β-catenin (red). The nuclei were stained by DAPI (blue). c Total cell lysates from five HCC cell lines were immunoprecipitated with an anti-TXNDC12 antibody or control IgG. The β-catenin and TXNDC12 levels are indicated. d 293T cells transfected with Flag-tagged full-length TXNDC12 or TXNDC12 fragments were immunoprecipitated with an anti-Flag antibody. The β-catenin and Flag-TXNDC12 (full-length or fragments) levels are indicated