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. 2019 Oct 4;14(10):e0223498. doi: 10.1371/journal.pone.0223498

Fig 2. CsBZIP40 localizes to the nucleus.

Fig 2

(A) Prediction of nuclear localization with CELLO and NLS. (B) Plasmid structure for transient expression to detect the subcellular localization of CsBZIP40. LB: left border, RB: right border. Fluorescent signals of GFP in onion epidermal cells (C) were used as the control. (D) The transient expression measured by CsBZIP40-GFP fluorescence. In C and D, scale bar represents 50 μm. Each field of view was observed in dark field (DARK), bright-field (BRIGHT) and merged imaging of bright and dark fields (MERGE).