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. 2019 Mar 6;19(5):3584–3592. doi: 10.3892/mmr.2019.10012

Table I.

Polymerase chain reaction primers used in this study.

Gene Primer sequences (5′-3′) Product size (bp)
H-ISL-1 181
  Forward GCGGCAATCAGATTCACGAT
  Reverse GCGCATTTGATCCCGTACAA
H-Tbx18 173
  Forward TCCAAGGTACTGGGAATGGC
  Reverse TGTGCTGTATCGGTTGAGGG
R-HCN4 300
  Forward GCATCCACGACTACTACGAAC
  Reverse TCTCCTTGTTGCCCTTAGTG
R-cTnT 202
  Forward GCAGGCTCTTCATGCCCAACT
  Reverse CGCTCTGCCCGACGCTTTT
R-Tbx3 168
  Forward TTACAGCCCGTATTCCATCCC
  Reverse CGGCTATTCAGTTCCGACCC
R-Nkx2.5 248
  Forward ACGCCCTTCTCAGTCAAAGA
  Reverse TAAAATGTAGGGGCGGTTGG
R-Cx43 242
  Forward GGCAAGGTGAAAATGAGGGG
  Reverse AAAGCGAGAGACACCAAGGA
R-Cx45 112
  Forward TTCTGATAATGTATGGTGTC
  Reverse AGTTCCCTCCTTTTACTGTT
R-GAPDH 253
  Forward ACAGCAACAGGGTGGTGGAC
  Reverse TTTGAGGGTGCAGCGAACTT

H-ISL-1, human insulin gene enhancer binding protein 1; H-Tbx18, human T-box 18; R-HCN4, rat hyperpolarization-activated cyclic nucleotide-gated potassium channel 4; R-cTnT, rat cardiac troponin T; R-Tbx3, rat T-box 3; R-Nkx2.5, rat homeobox protein Nkx-2.5; R-Cx43, rat connexin 43; R-Cx45, rat connexin 45.