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. 2002 Jun 3;21(11):2692–2702. doi: 10.1093/emboj/21.11.2692

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Fig. 7. Gene expression pattern and enolase activity of LOS2. (A) Expression of the LOS2 gene transcript. Full-length LOS2 cDNA was used as a probe. The β-tubulin gene was used as a loading control. (BLOS2 promoter::GUS expression. Wild-type plants containing LOS2 promoter::GUS were stained with X-Gluc for 15 h and visualized under a microscope. (C) Immunoblot analysis. A 20 µg aliquot of total protein from wild-type and los2 leaves was extracted and fractionated in a 12.5% SDS–polyacrylamide gel. Shown are the gel picture of Coomassie staining and immunodetection with polyclonal anti-enolase. Molecular size markers are shown on the left. (D) Wild-type and mutant enolase activity. Shown are the mean values ± SE from three replicates.