erse Transcription Kit following the manufacturer's directions. cDNA was subsequently subjected to qPCR on a CFX-96 True Time Program employing the iQ SYBR GREEN SUPERMIX. The PCRs have been cycled 40 times right after initial denaturation with all the following parameters: 95uC for 10 s, annealing and extension at 60uC for 30 s. For each experiment, a non-template reaction was applied as a negati
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