Quantitative real-time PCR (qPCR) is a powerful tool to measure gene expression levels.
Accurate and reproducible results are dependent on the correct choice of the reference
genes for data normalization. To date, screenings evaluating candidate reference gene
stability for expression studies in maize have not been reported. In the present work, we
analyzed the expression patterns of 12 genes in a set of 20 maize samples, obtained from
different tissues of plants grown at various experimental conditions. Using genormPLUS …