Total RNA isolation was performed according to Wan et al. [46 (link)]. Gene-specific primers for RT–qPCR were designed using Primer 5, and the primer sequence is given in Supplementary Data Table S7. Gene expression analysis of CsLOXs was performed using SYBR Green in a BioRad IQ5 PCR thermal cycler (Bio-Rad, USA). The associations between CsLOX gene expression and alcohol content were investigated using Graphpad Prism 5.0 (GraphPad Software Inc., La Jolla, CA, USA).
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