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. 2016 Feb 3;6:20582. doi: 10.1038/srep20582

Figure 9. qRT-PCR validation of transcript levels evaluated by RNA-Seq in roots and leaves of G. davidsonii under 200 mM NaCl stress conditions.

Figure 9

(A,B) represent the correlation of the fold change analyzed by RNA-Seq platform (x-axis) with data obtained using real time PCR (y-axis) in roots and leaves of G. davidsonii. 30 independent genes were randomly selected: 10 up-regulated genes, 10 unchanged genes and 10 down-regulated genes. Three biological replicates were used from each sample at five time points post salt stress.