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. 2005 Jul;138(3):1563–1576. doi: 10.1104/pp.105.062562

Figure 3.

Figure 3.

Northern-blot analysis of RsBGAL1. Total RNA was extracted from young leaves, hypocotyls, and roots and then subjected to northern hybridization using the labeled RsBGAL1 fragment excised from RsBGAL1 cDNA as the probe. The position of the segment excised from the hypocotyls for RNA preparation is indicated in parentheses (distance from the cotyledons). The methylene blue-stained 18S rRNA used as a loading control is shown at the bottom.