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. 2023 Feb 16;24(4):4000. doi: 10.3390/ijms24044000

Table 1.

PCR primers used for this study.

Primer Sequence (5′-3′)
ATP1A1-F a CGGGGTACCATGGGGAAGGGGGTTGGAC
ATP1A1-CT-F a CGGGGTACCATGCTGGATGACAACTTCGCCTC
ATP1A1-1R a CGGGATATCCTAGGCTTGCTGAGGAACCATGTTTTTG
ATP1A1-2R a CGGGATATCCTACACTGCCCTGTTACAAAGACCTG
ATP1A1-3R a CGGGATATCCTAGGCATCCCTGGGGTTCACC
ATP1A1-4R a CGGGATATCCTAGACGGTGCCCAGGGG
ATP1A1-R a CGGGATATCCTAGTAGTAGGTTTCCTTCTCCACCC
PEDV-N-F b ATGATCTGGTGGCTGCTGTC
PEDV-N-R b CTTCGAAGTGGCCCTGGATT
Porcine-ATP1A1-F b CTTGAGCCGAGGCTTAACAC
Porcine-ATP1A1-R b GAATGCCATAGGCCAAGAAA
Monkey-ATP1A1-F b CAGCAGTGGACCTATGAGCA
Monkey-ATP1A1-R b CATTCCAGGGCAGTAGGAAA
Porcine-GAPDH-F b GATGCTGGTGCTGAGTATGT
Porcine-GAPDH-R b GGCAGAGATGATGACCCTTT
Monkey-GAPDH-F b CGAGATCCCTCCAAAATCAA
Monkey-GAPDH-R b TGACGATCTTGAGGCTGTTG

a The target genes were amplified by PCR and cloned into the KpnI (bold) and EcoRV (red) sites in the pECMV-3×FLAG-N vector. b Used for relative quantitative PCR.