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. 2016 Mar 19;67(10):3165–3175. doi: 10.1093/jxb/erw118

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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. 3. — Subcellular localization studies of CmGOX. (A) Localization of CmGOX in C. merolae. Red: chloroplast autofluorescence; blue: DAPI-stained nucleus; green: YFP signal from YFP::CmGOX construct. C. merolae cells were transformed 24h before microscopic analysis. (B) Localization of CmGOX in tobacco protoplasts. From left to right: YFP signal of YFP::CmGOX construct, chlorophyll autofluorescence, CFP signal as peroxisomal marker (CFP::PTS1), and merge of all three pictures. Microscopic analyses were performed with protoplasts isolated from transiently transformed N. benthamiana leaves.