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. 2018 Nov 1;18:265. doi: 10.1186/s12870-018-1494-z

Fig. 9.

Fig. 9

qRT-PCR analysis of VcRR2 in Mu-Legacy and Mu-Legacy-T1 using E1F and E1R primers. Eukaryotic translation initiation factor 3 subunit H is the internal control. Log2(fold-change) in Legacy-VcDDF1-OX was calculated by -∆∆Ct = −[(CtGOI – Ctnom)Mu-Legacy or Mu-Legacy-T1 – (CtGOI – Ctnom)Legacy]. Average fold-changes ± standard deviation of three biological replicates for each of Mu-Legacy, Mu-Legacy-T1, and nontransgenic ‘Legacy’ plants were plotted. Significant average fold-change determined using a Student’s t-test is denoted. Asterisks (**) indicate p < 0.01. The fold change of RNA-seq is an average of the Log2Fold change (Mu-Legacy/Legacy) for three DE isoforms listed in Table 1