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. 2016 Aug 19;67(17):5051–5066. doi: 10.1093/jxb/erw273

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© The Author 2016. Published by Oxford University Press on behalf of the Society for Experimental Biology.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Fig. 6. — Bimolecular fluorescence complementation (BiFC) visualization of TCP dimerization in transiently transfected P. aphrodite petal protoplasts. (A–D) Co-expression of non-fused YN with non-fused YC was unable to reconstitute a fluorescent YFP chromophore. (E–H) Co-expression of non-fused YN with YC-PePCF10 was also unable to reconstitute a fluorescent YFP chromophore. (I–L) PeTCP10 interacts with PeTCP10 protein in nucleus of flower cell. (M–P) Co-expression of non-fused YN with YC-PeCIN8 was also unable to reconstitute a fluorescent YFP chromophore. (Q–T) PeCIN8 interacts with PeCIN8 protein in nucleus of flower cell. (U–X) Co-expression of YN-PeCIN8 with YC-PePCF10 was unable to reconstitute a fluorescent YFP chromophore. The fluorescence indicates interaction between the indicated partner proteins. The images were obtained from the yellow fluorescent protein channel or bright field or are a merged image of the yellow fluorescence, and cells stained with PI represented in red. Scale bars: 20 μm.