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. 2020 Mar 25;37(1):25–30. doi: 10.5511/plantbiotechnology.19.1209a

Figure 1. Outline of the plate assay for regeneration efficiency of potato cultivars. (A) Schematic representation of the regeneration procedure from potato cultured cells using a 24-well culture plate. (B) Layout of the 24-well culture plate. Each well contains a culture medium containing various concentrations of IAA and tZR, ranging 0 to 1.06 mg l−1 and 0 to 28 mg l−1, respectively. (C–E) Photographs of sections of ‘Konafubuki’ stems after 30-day culture. Panels indicate the cells without shoot regeneration (C), and those showing regenerated shoot (D, E). Scale bars indicate 5 mm.

Figure 1. Outline of the plate assay for regeneration efficiency of potato cultivars. (A) Schematic representation of the regeneration procedure from potato cultured cells using a 24-well culture plate. (B) Layout of the 24-well culture plate. Each well contains a culture medium containing various concentrations of IAA and tZR, ranging 0 to 1.06 mg l−1 and 0 to 28 mg l−1, respectively. (C–E) Photographs of sections of ‘Konafubuki’ stems after 30-day culture. Panels indicate the cells without shoot regeneration (C), and those showing regenerated shoot (D, E). Scale bars indicate 5 mm.