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. 2006 Apr;80(8):3994–4004. doi: 10.1128/JVI.80.8.3994-4004.2006

TABLE 1.

Primers used in this studya

Primer Nucleotide sequence
GP5-For 5′ GCCGGAATTCGGAGCCGCCGCCACCATGTTGGGGAGATGCTTGAC 3′
GP5-Rev 5′ CCCCGAATTCCTAAAGACGACCCCATTGTTC 3′
M-For 5′ ATATATGGATCCGCCACCATGGGGTCGTCTTTAGACGAC 3′
M-Rev 5′ ATATATGCATGCTTATTTGGCATATTTGACAAGG 3′
GP5-N34A-For 5′ GCCAACAGCGCCAGCAGCTCTC 3′
GP5-N44A-For 5′ GTTGATTTACGCCTTGACGCTATG 3′
GP5-N51A-For 5′ GTGAGCTGGCTGGCACAGATTG 3′
GP5-N34/44A-For 5′ GCCAACAGCGCCAGCAGCTCTCATCTTCAGTTGATTTACGCCTTGACGCTATG 3′
GP5-N44/51A-For 5′ GTTGATTTACGCCTTGACGCTATGTGAGCTGGCTGGCACAGATTG 3′
GP5-N34/51A-For 5′ GCCAACAGCGCCAGCAGCTCTCATCTTCAGTTGATTTACAACTTGACGCTATGTGAG CTGGCTGGCACAGATTG 3′
GP5-N34/44/51A-For 5′ GCCAACAGCGCCAGCAGCTCTCATCTTCAGTTGATTTACGCCTTGACGCTATGTGAG CTGGCTGGCACAGATTG 3′
PRRSV-13177-For 5′ CTACCAACATCAGGTCGATGGCGG 3′
PRRSV-14473-Rev 5′ GTCGGCCGCGACTTACCTTTAGAG 3′
a

Underlining indicates mutations. Restriction enzyme sites incorporated in the primers are shown in bold; the initiation codons for the GP5 and M proteins are shown in bold italics.