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A, DNA gel-blot analysis to verify the specificity of the various XTR gene-specific probes. Entire cDNA clones were used as probes. Hybridization was carried out under stringent conditions in solution containing sodium phosphate at 65°C. B, Organ-specific expression of rice XET-related genes. Each lane contained 10 μg of total RNA isolated from the indicated organ. Hybridization was carried out under stringent conditions with Denhardt's solution at 65°C.
