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/ml, respectively made up to 200 l using Tris-EDTA buffer. The suspensions
/ml, respectively made up to 200 l using Tris-EDTA buffer. The suspensions were vortexed for 10 s and incubated at room temperature for 10 min with 2 min mixing interval. RNA extraction of the treated cells was performed using RNeasy Plus Mini kit (Qiagen, Germany) according to manufacturer's guidelines and eluted in DEPC water (Bioline, UK). A total of three biological replicates were included fo