“…The cDNA was diluted 20 times and a 0.6 µL aliquot was used in a 15 µL quantitative PCR (qPCR) reaction mix: 0.45 µL SYBR Green I dye (Invitrogen, Grand Island, NY), 1× iTaq buffer (Biorad, Hercules, CA), 0.2 mM dNTP (Applied Biosystem, Waltham, MA), 2.5 mM MgCl 2 , 0.3 units of iTaq DNA polymerase (Biorad, Hercules, CA) and 0.2 µM forward/reverse primer (IDT, Coralville, IA). Quantitative reverse transcription PCR (qRT-PCR) amplification and detection was performed as described [12]. Dissociation curves were run for each primer set to verify the specific amplification.…”