Total RNA from the TRs at 50 DAT and 95 DAT were extracted using RNA plant kits (Tiangen, DP441-50T), and then reverse transcribed, and the synthetic cDNA was used for qPCR. In this study, each qPCR result had three biological replications. The primers in this study were shown in Supplementary Table S1. The reference gene was GAPDH, and the relative expression levels related in sucrose-starch metabolism were analyzed using the 2−ΔΔCT method [45 (link),46 (link)].
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