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. 2016 Nov 15;10:523. doi: 10.3389/fnins.2016.00523

Table 1.

Primers used for RT-PCR and qPCR analysis.

Gene Sequence
Oct4 Forward TCTTTCCACCAGGCCCCCGGCTC
Reverse TGCGGGCGGACATGGGGGAGATCC
Nanog Forward GACTGAGATATGGCTTGCTC
Reverse CTTTCTGAGGGATAGGGTCT
Klf4 Forward GGCGAGTCTGACATGGCTG
Reverse GCTGGACGCAGTGTCTTCTC
Pax6 Forward CGGAGGGAGTAAGCCAAGA
Reverse AAGGGCACTCCCGTTTATACT
Lin28 Forward AGGCGGTGGAGTTCACCTTTAAGA
Reverse AGCTTGCATTCCTTGGCATGATGG
Sox2 Forward TAGAGCTAGACTCCGGGCGATGA
Reverse TTGCCTTAAACAAGACCACGAAA
C-myc Forward TGACCTAACTCGAGGAGGAGCTGGAATC
Reverse AAGTTTGAGGCAGTTAAAATTATGGCTG
DNMT1 Forward CCTAGTTCCGTGGCTACGAGGAGAA
Reverse TCTCTCTCCTCTGCAGCCGACTCA
DNMT3a Forward GCCGAATTGTGTCTTGGTGGATGACA
Reverse CCTGGTGGAATGCACTGCAGAAGGA
DNMT3b Forward TGGGTACAGTGGTTTGGTGA
Reverse GCCCTTGTTGTTGGTGACTT
Gadd45a Forward CCTGCACTGTGTGCTGGTGA
Reverse CCACTGATCCATGTAGCGACTTTC
Gadd45b Forward CCTGGCCATAGACGAAGAAG
Reverse AGCCTCTGCATGCCTGATAC
Tet1 Forward GAGCCTGTTCCTCGATGTGG
Reverse CAAACCCACCTGAGGCTGTT
Tet2 Forward GCCATTCTCAGGAGTCACTGC
Reverse ACTTCTCGATTGTCTTCTCTATTGAGG
Tet3 Forward GGTCACAGCCTGCATGGACT
Reverse AGCGATTGTCTTCCTTGGTCAG
GAPDH Forward ACTGGCATGGCCTTCCGTGTTCCTA
Reverse TCAGTGTAGCCCAAGATGCCCTTC