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. 2015 Apr 2;10(4):e0122072. doi: 10.1371/journal.pone.0122072

Fig 6. (A) Gene expression data for digital gene expression analysis.

Fig 6

The fold changes of the genes were calculated as the log2 value of each empty/full comparison and are shown on the y-axis. (B) The quantitative real-time PCR analysis of gene expression data. Quantitative variation of ABF, ERF1, CTR1, ERF2, EIN3, PYL, SUPT5H and TRA2 in Empty were compared with Full, and β-Actin (GenBank: AB298788) was used as the internal standard.