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. 1998 Jan;116(1):27–35. doi: 10.1104/pp.116.1.27

Figure 2.

Figure 2

RNA gel-blot hybridization analysis of PNZIP mRNA accumulation in different P. nil organs. Each lane contained 30 μg of total RNA isolated from cotyledons, hypocotyls, or roots. Hybridization to a ubiquitin cDNA probe served as a control for equal loading of RNA in each lane. Numbers on the right indicate the approximate sizes of the mRNAs detected.