RNA isolation and reverse transcription reaction were performed as previously described in Kim et al. (2019 (link)). RNA extraction was done from p9 whole brain tissue of WT and BDNF+/– mice using RNAqueous kit with no alterations to procedure (AM1931, Thermofisher). qPCR was executed using 7900HT Fast Real-Time PCR system (Applied Biosystems), data were analyzed using SDS v2.4 (Applied Biosystems). GAPDH was used as a reference housekeeping gene. Delta (Δ) CT (MeanGene- MeanGAPDH) was utilized to calculate ΔΔCT (ΔCTPos-ΔCTNeg), and data was normalized to WT (100%). Mouse primers used: BDNF Forward: 5’-TCGTTCCTTTCGAGTTAGCC, BDNF Reverse: 5’-TTGGTAAACGGCACAAAAC, GAPDH Forward: 5’-AGTATGACTCCACTCACGGCAA, and GAPDH Reverse: 5’-TCTCGCTCCTGGAAGATGGT.
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