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. 2019 Aug 14;317(5):C881–C893. doi: 10.1152/ajpcell.00205.2019

Table 2.

Sus scrofa forward and reverse primer sequences used for RT-PCR with corresponding product sizes (bp)

Primer Sequence 5′–3′
Sus Scrofa Gene Protein Forward Primer Reverse Primer Product Size, bp
Il1r1 IL1R1 TTACACAGAGACTACCGGTTGC CAGTTTTATCACCCGGGAGACA 263
Il1r2 IL1R2 AAATGATTCCACGACCATCCCA TCCCAAAACCAGGATGATGAGG 874
Tnfrsf1a TNFRSF1A GAAACAGGACACCATCTGCAAC AAGCTAAGCCAACGAAGAGGAA 218
Tgfbr1 TGFBR1 GAGACAGGCCATTTGTATGTGC TAAATCTCTGCCTCACGGAACC 520
Tgfbr2 TGFBR2 GGAAGCTGATGGAGTTCAGTGA TCTCTGTCTTCCAGGAGGCATA 252
Tgfbr3 TGFBR3 ATATTCACCACAAGCCTGTCGT ATACTCCTTTCGGGCCCAATTT 224
Il6r IL6R AAGATTCTGCGTCGGTACCATT TGTTGCTGACATCATAAGGGCT 312
Il10ra IL10RA GGATGAAGTGACTCTGACGGTT GCTTCACCCTGACACACAATTC 257
Il4r IL4R AGAGCTACCTGTACTCGGAACT CCCTTTGTCTTCCTCCTCTTCC 695
Tlr1 TLR1 TGTCCCACAACAAGTTGGAGAA TTGTGGGAAACTGAACACCTCA 650
Tlr2 TLR2 TCCCAAATCTGCGAATCCTGAA ATGCAACCTCCGGACTGTTAAT 512
Tlr3 TLR3 CGATGACCTCCCGGCAAATATA GAGATTTTCCAGTTGGAGCTGC 382
Tlr4 TLR4 TTCTCTCCTGCCTGAGATCTGA ACTCCAGGTAGGTATTCCTGCT 555
Tlr5 TLR5 TCCTGTGGTCTCTCTGATGCTA GGGTTCATACACTTCCCCCAAT 284
Tlr6 TLR6 AGACAATCTTGTGCCATCCCAT GGCCCTTGAGTGAGTTCCAATA 409
Tlr7 TLR7 GACACTAAAGACCCAGCAGTGA CTGAAGGGGCTTCTCAAGGAAT 297
Tlr8 TLR8 CTGAGGCAGAACAGGATTTCCT TTCATCACCCAGTCTGTGACAG 542
Tlr9 TLR9 GCCTACGAACTCTCAACCTCAA GGAAGTTCTCACTCAGGTCCAG 696
Tlr10 TLR10 TCAGGTGCTTGCCCAGAAATAT TCTTGCCAGGATCAGAGTTTCC 717
Cyp2c42 CYP2C42 TCCTGTCTGCTTCTCCTTTCAC GGGAGCACAGTCCAGGATAAAA 489
Cyp2e1 CYP2E1 TCGAGATTTCACTGACACCCTG GTTAAAGTGCTGCAAGATGGCA 592
Alox5 5-LOX TGACAGTGGATGAAGAACTGGG TGTTTTTGCCGTGTTTCCAGTT 259
Alox12b 12R-LOX ACACCATCCAGATCAACAGCAT CCAGAGGACCAATAGGACGATG 602
Alox15 12/15-LOX CAGGAGGATGAACTCTTTGGCT TCGAATATACCTCCGTCCGAGA 578
Alox15b 15-LOX2 GCGAAATGCTGAGTTCTCCATC CAGGGTGGAATAGTTCAGCTGT 283
Cox1 COX1 TCACCCGCAATACTATGAGCTC TGTGTGATAGGGAGGAGGACAT 510
Cox2 COX2 CCCTTTCCAACTAGGCTTCCAA TAGTCGTCCTGGGATAGCATCT 529
Gapdh GAPDH TTTTAACTCTGGCAAAGTGGAC CATTGTCGTACCAGGAAATGAG 884

Three different primer sets were generated and tested for each gene. Primers included in this table were utilized for Fig. 1, AC. GAPDH was used as a positive control.