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. 2018 Jul 24;12:35. doi: 10.3389/fnsys.2018.00035

Table 1.

RT-qPCR primer and probe sequences used for amplification of cDNA.

Gene Forward primer sequence Reverse primer sequence
GAPDH 5′-AGAAGGTGGTGAAGCAGGCATC-3′ 5′-CGAAGGTGGAAGAGTGGGAGTTG-3′
β-Actin 5′-TCGTGATGGACTCCGGTGAC-3′ 5′-TCGTGGATGCCACAGGACTC-3′
Pgk1 5′-GTCGTGATGAGGGTGGACTT-3′ 5′-TTTGATGCTTGGAACAGCAG-3′
CREB 5′-GCTTATTCTGGTGAGTACTAAGTCTTAATGAGT-3′ 5′-GACAAAAGTCTTTATTTATTAACACCTTATTG-3′
Arc 5′-CTCAGAGGAGTTCTTAGCCTGTTCG-3′ 5′-ATCTCAGCTCGGCACTTACCAAT-3′
BDNF 5′-TGAGCGTGTGTGACAGTATTAGCG-3′ 5′-CATGGGATTACACTTGGTCTCGTAG-3′
Egr-1 5′-GTTCCCATGATCCCTGACTATCTG-3′ 5′-GACTGAGTGGCGAAGGCTTTAATA-3′
c-fos 5′-TTTCAACGCGGACTACGAGG-3′ 5′-GCGCAAAAGTCCTGTGTGTT-3′
Npas4 5′-AGCAAGAGCCTGAGCGAAAAGA-3′ 5′-CTTGGTGGATCGGTACATGACTG-3′