Taqman custom rt pool

Expression levels of miRNAs were detected by RT-qPCR. Briefly, a fixed volume of 3 μL of miRNA solution was used for reverse transcription using a TaqMan MicroRNA Reverse Transcription Kit and the TaqMan Custom RT pool (Applied Biosystems, CA, USA). For our custom selection, 3.125 μL of reverse transcription reaction was used for preamplification with TaqMan PreAmp Master Mix (2X) and the TaqMan PreAmp pool (Applied Biosystems, CA, USA). The preamplification reaction was diluted with water (1:130) and 5 μL was used for RT-qPCR with TaqMan Universal Master Mix II, no UNG and specific TaqMan MicroRNA assays (Applied Biosystem, CA, USA). Reverse transcription and preamplification reactions were carried out as mentioned above. RT-qPCR reaction was performed with an Applied Biosystems QuantStudio 7 under the following conditions: 50 °C for 2 min, followed by 40 cycles of 95 °C for 15 s and 60 °C for 1 min. The results were normalized using the best ECs identified together with the spike-in control (cel-miR-39-3p).

Expression profiling of 188 miRNAs identified as the most consistent and reliable miRNAs in human plasma^{14 (link)} was performed using TaqMan-Low-Density-Array (TLDA) human custom arrays as instructed by the manufacturer (Applied Biosystem, CA, USA) with Applied Biosystems QuantStudio 7. Briefly, a fixed volume of 3 μL of miRNA solution was used for reverse transcription using a TaqMan MicroRNA Reverse Transcription Kit and the TaqMan Custom RT pool (Applied Biosystems, CA, USA), which were customized for TLDAs. The reaction was performed under the following conditions: incubation for 30 min at 16 °C and 30 min at 42 °C, inactivation for 5 min at 85 °C and immediate cooling to 4 °C. The cDNA was stored at − 20 °C. For our custom selection, 3.125 μL of the reverse transcription reaction was used for preamplification using TaqMan PreAmp Master Mix (2X) and TaqMan PreAmp pool (Applied Biosystems, CA, USA). The reaction conditions were as follows: 10 min at 95 °C, 2 min at 55 °C, 2 min at 72 °C, 12 cycles of 15 s at 95 °C and 4 min at 60 °C, inactivation for 10 min at 99.9 °C and cooling to 4 °C. The preamplification reaction was then diluted with water (1:3), and 4.5 μL was used for TLDA. Reverse transcription and preamplification reactions were carried out with an Applied Biosystems Verity Thermal Cycler. Data were normalized by the mean-centre normalization method.