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. 2007 Oct;145(2):450–464. doi: 10.1104/pp.107.106021

Figure 1.

Figure 1.

Phenotypic and molecular characterization of gh3.5-1D. A, T-DNA insertion in gh3.5-1D. The large arrow indicates the GH3.5 gene. The four cauliflower mosaic virus 35S enhancer elements are indicated with small arrowheads. B, Four-week-old Col-0, heterozygous (gh3.5-1D+/−), homozygous (gh3.5-1D/−), and representative p35SGH3.5 transgenic plant. C, Northern-blot analysis (top) of GH3.5 expression and western-blot detection (bottom) of the GH3.5 protein in Col-0, gh3.5-1D+/−, gh3.5-1D/−, and p35SGH3.5 plants. Rubisco staining was used as a loading control in western blots. The experiments were repeated at least once with similar results.