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Expression of AtSNAP33 and PR1 transcripts 1 and 2 d after treatment with 330 μm BTH or 330 μm or 1 mm SA. Wetting powder (WP) or water were used as a control for BTH or SA, respectively. Leaves were collected, the RNA was extracted, and AtSNAP33 and PR1 mRNA levels were detected by RNA-blot hybridization. The RNA gel stained with ethidium bromide is shown as a control for loading.
