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. 2017 Sep 13;7:11443. doi: 10.1038/s41598-017-11936-0

Figure 4.

Figure 4

Integration and expression of the GFP gene in transgenic ‘Haruyokoi’. (a) Genomic polymerase chain reaction (PCR) analysis of four T1 transgenic (HG1–4) lines and wild-type (Wt) plants. Genomic DNA was extracted from each first leaf. The full-length gel image is shown in Supplementary Fig. S5. (b) Reverse transcription-PCR (RT-PCR) analysis of GFP expression in HG1–4 lines and Wt plants. The GAPDH gene was used as a housekeeping control. Full-length gel images are shown in Supplementary Fig. S6. (c) DNA gel blot analysis of transgenic wheat lines (T2 progeny) and Wt lines using genomic DNA from leaves digested with HindIII. Two-hundred picograms of the linearised GFP vector (5.1 kb) used as a positive control (P).