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. 2021 Jan 26;11:2187. doi: 10.1038/s41598-021-81276-7

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© The Author(s) 2021

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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Visualization of protein–protein interaction of the AtUBP-24 with the various AtG3BPs and PNYDV Clink via bimolecular fluorescence complementation (BiFC) under ambient conditions and heat shock (45 min at 37 °C). (a) Interaction of AtUBP-24 with the corresponding partners fused C-terminally with splitYFP. (b) Interaction of AtUBP-24 and the respective AtG3BPs and PNYDV Clink N-terminally fused to splitYFP. All pictures are projections of z-stacks obtained by confocal laser scanning microscopy. The individual pictures correspond to a size of 185 × 185 µm.