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Subcellular localization of seven fluorescent LFMADS-mGFP proteins. Recombinant plasmids harboring a C-terminal mGFP fusion with LFMADSs were driven by the CaMV 35S promoter (35S::LFMADSs-mGFP). These seven recombinant proteins were transiently expressed in lily tepal by using the particle bombardment method. The NLS domain of VirD2 fused with mCherry in this study was used as the nuclear marker control. Overlay (merge) images are shown in the extreme right column. Bar = 20 μm.
