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. 2013 Jun 18;8(7):e24793. doi: 10.4161/psb.24793

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Figure 4. Topographic fluorescence analysis of red beet protoplasts isolated from tissue incubated 24 h in 200 mM sucrose at two different stages. (A) Protoplast from dormant beet hypocotyls with a large central vacuole. (B) Protoplast from tissue incubated in 200 mM sucrose for 24 h. Fluorescence intensity of vacuole-derived vesicles is similar to that emanating from the vacuole.