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. 2020 Sep 24;10:15711. doi: 10.1038/s41598-020-72594-3

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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 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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Comparison of subcellular localization of P-STAT3^Ser727 in AGS cells infected with H. pylori. AGS cells were co-cultured with H. pylori and harvested at indicated time points. (A) Western blot analysis of P-STAT3^Ser727, P-STAT3^Tyr705 and STAT3 in cytosolic and nuclear extracts. Lamin B and α-tubulin were used as nuclear and cytoplasmic protein markers, respectively. (B) Western blot analysis of P-STAT3^Ser727 and STAT3 in cytosolic and mitochondrial extracts. VDAC and α-tubulin are mitochondrial and cytoplasmic protein markers, respectively. (C) Verification of mitochondrial translocation of P-STAT3^Ser727 upon H. pylori infection for 12 h. Mitotracker was used as a selective probe of mitochondria. Scale bar, 100 μm.