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. 2004 Nov;52(11):1483–1493. doi: 10.1369/jhc.4A6306.2004

Table 2.

Primer sets used for RT-PCR of MCT1, MCT2, and MCT4 a


MCT Primers Sequence Total bp Coding bases

MCT1 P1 GGAGGTCTTGGGCTTGCCTTCAACT 799 358-382
P2 GGACTCTTTGCACCTTTGGTGT 331 826-847
P3 GGATTCTGTGTCTATGCGGGATTC 94 1063-1086
RP1 CAACAAGGTCCATCAATGTTTCAA 1157-1134
MCT2 P1 CGGGCGCCCACCCTGCGCCAGAGACCAG 650 (−161)-(−134)
P2 TAATTGGCAAATACTTCTATAGGAAGCG 636 401-428
RP1 AGGAGCCAATGAACTTAAGAAAACAGGA 489-462
RP2 AATACAGCATATAATACCAGGCTTGT 1037-1012
MCT4 P1 GGCGAGAGGCGGGCTGAGGCGGCCCAG 582 (−62)-(−36)
P2 CCCTGTCTTCCTGTGTGCCCTGAG 601 468-492
P3 CCATCGTGGGCACCCACAAGTTCT 419 1034-1057
RP1 AGCGGTCCTGCAGCAGCTGCCCCAGCG 520-594
RP2 CAATGGCACTGGAGAACTTGTGGG 1069-1046
RP3 AAGCGTTGCCGGCTTCTGTACCTC 1453-1430

aThe correspondingly numbered P and RP were used as primer pairs for each amplification except for MCT1, where one RP was used for all. P is a forward primer (5′ × 3′) and RP is a reverse primer (3′ × 5′). The coding bases count from the start codon's first nucleotide. Nucleotides in parentheses precede the coding region counting 5′(−) backward before the first coding base. Total bp listed in column 4.