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. 2018 Oct 9;8:15034. doi: 10.1038/s41598-018-33102-w

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© The Author(s) 2018

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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Co-localization analysis of FluoZin-3 and three vesicular markers demonstrates that FluoZin-3 non-specifically localizes to lysosomal, Golgi, and secretory vesicles. (a) Representative fluorescence images of Spirozin2-stained cells, vesicular markers- FP, and the merged channel. (b) Pearson coefficient plot of co-localization analysis. A minimum of 18 cells were analyzed for each condition. Scale bar, 5 μm.