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erse Transcription Kit following the manufacturer's instructions. cDNA was subsequently subjected to qPCR on a CFX-96 Genuine Time Technique using the iQ SYBR GREEN SUPERMIX. The PCRs have been cycled 40 times following initial denaturation with all the following parameters: 95uC for ten s, annealing and extension at 60uC for 30 s. For every single experiment, a non-template reaction was used as a
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