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. 2019 Sep 10;10(9):659. doi: 10.1038/s41419-019-1879-4

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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. 6 — a Nuclear extracts were prepared from human melanoma cells and were incubated with tryptase as indicated, followed by SDS-PAGE analysis and Coomassie staining. The major bands affected by tryptase (arrows) were identified as hnRNP A2/B1 and Lamin B1, respectively. b–d Western blot analysis of hnRNP A2/B1 and Lamin B1 in tryptase-treated nuclear extracts. Quantification of the Lamin B1 and hnRNP A2/B1 bands by densitometric scanning is shown in (c) and (d), respectively. e–g Western blot analysis of hnRNP A2/B1 and Lamin B1 in tryptase-treated cells. Quantification of the Lamin B1 and hnRNP A2/B1 bands by densitometric scanning is shown in (f) and (g), respectively. h Recombinant hnRNP A2/B1 was treated with tryptase, followed by SDS-PAGE and Coomassie staining