Primer sets used for quantitative real-time PCR of differentially expressed genes (DEGs) identified from RNA-Seq between normal and stem browning samples of the mushroom Lentiula edodes

Based on the results of the RNA-Seq analysis of black and normal stems in Lentinula edodes, quantitative reverse-transcription PCR (qRT-PCR) was performed to confirm the expression levels of 17 differentially expressed genes (DEGs) annotated as transcription factors and oxidoreductases. The primer sets used during this process are shown in this Table.