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Subcellular localization of mobilization-defective bZIP17. Arabidopsis leaf protoplasts were cotransformed with YFP-bZIP17(fl) or YFP-bZIPG372A and with either RFP-tagged ER markers (A and C) or Golgi markers (B and D; Nelson et al., 2007). Protoplasts were treated overnight with 2 mM DTT to induce ER stress, and protoplasts were observed by confocal microscopy. Bars = 10 μm.
