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. 2017 Nov 28;8:271. doi: 10.1186/s13287-017-0720-1

Table 1.

Primers used for RT-PCR and qRT-PCR analysis

Gene Forward primer Reverse primer
GAPDH TCCTCTGACTTCAACAGCGA GGGTCTTACTCCTTGGAGGC
CCNA2 CAGCCAGACATCACTAACAGT CCCACAAGCTGAAGTTTTCCT
CCNB1 GTTGGTGTCACTGCCATGTT TGGCCAAAGTATGTTGCTCG
CCND1 GTCTGCGAGGAACAGAAGTG GGATGGAGTTGTCGGTGTAG
CCNE1 GGAAGAGGAAGGCAAACGTG GCAATAATCCGAGGCTTGCA
OCT4 GACAGGGGGAGGGGAGGAGCTAGG CTTCCCTCCAACCAGTTGCCCCAAAC
c-MYC AGAAATGTCCTGAGCAATCACC AAGGTTGTGAGGTTGCATTTGA
REX1 ACCAGCACACTAGGCAAACC TTCTGTTCACACAGGCTCCA
KLF4 ATAGCCTAAATGATGGTGCTTGG AACTTTGGCTTCCTTGTTTGG
NANOG TGCAAGAACTCTCCAACATCCT ATTGCTATTCTTCGGCCAGTT
SeV* GGATCACTAGGTGATATCGAGC ACCAGACAAGAGTTTAAGAGATATGTATC
KOS-tg* ATGCACCGCTACGACGTGAGCGC ACCTTGACAATCCTGATGTGG
Klf4-tg* TTCCTGCATGCCAGAGGAGCCC AATGTATCGAAGGTGCTCAA
cMYC-tg* TAACTGACTAGCAGGCTTGTCG TCC ACATACAGTCCTGGATGATGATG
SOX7 TGAACGCCTTCATGGTTTG AGCGCCTTCCACGACTTT
HAND1 CCAGCTACATCGCCTACCTG CCGGTGCGTCCTTTAATCCT
ACTA2 GTGATCACCATCGGAAATGAA TCATGATGCTGTTGTAGGTGGT
MYL2 TACGTTCGGGAAATGCTGAC TTCTCCGTGGGTGATGATG
NESTIN CAGCGTTGGAACAGAGGTTGG TGGCACAGGTGTCTCAAGGGTAG
BMP4 CCTGTTGTGTGCCCACTGAAC ATCTCAGCGGCACCCACAT

*Used for SeV genome and transgene detection in cells reprogrammed using CytoTune 2.0 Sendai vectors (Thermo Scientific)

qRT-PCR quantitative reverse transcription PCR, RT-PCR reverse transcription PCR