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. 2016 Apr 14;12(4):e1005991. doi: 10.1371/journal.pgen.1005991

Fig 2. Sub-cellular localization and transactivation identification of ZmMADS47.

Fig 2

A. Schematic representation of multiple truncated ZmMADS47 constructions. B. Fluorescence signal resulting from expression of ZmMADS47 (FL)-CFP, ZmMADS47 (MADS)-CFP and CFP alone. Signal from CFP, DIC (differential-interference microscope) and merging the two signals are shown in these panels. Bar represents 50μm. C. The β-galactosidase activity resulting from the TF transactivation. O2 was used as a positive control, while the pGBK-T7 vector alone was used as a negative control. Error bars represent SD (n = 3) (***P < 0.001, Student’s t test).