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. 2004 Mar;78(6):2770–2779. doi: 10.1128/JVI.78.6.2770-2779.2004

TABLE 1.

Oligonucleotide primers utilized in plasmid constructions in this study

Name Sequence (5′→3′)a
B13RF TACACGACCAAGATCTATTACTATG
B13RR TGAAAAGACGTGGGTACCAAAGTT
B22RF GGTGGATCCCATGGATATCTTTAAA
B22RR TATCAGATCTAGTTTATACTATTAC
pUC18F TTCTTAGATCTCAGGTGGCACTT
pUC18/B13RR AATACGGGTACCCACAGAATCAGG
pUC18/B22RR ACAGAACCATGGGATAACGCAGG
p2B8RF TAACAAACTAGTCCATAAGATCT CCC
p2B8R/B13RR TTGTTTGTCGACTCTTATTATTTTTGACAC
p2B8R/B22RR GTTTGCGGTACCTTATTATTTTTGACAC
gptF ATAAACACCCGGGGACACTTCACAT
gptR ACAACGCCCGGGAGTGCCAGG
gptS1 AATATGAAAGTGGTGATTGTGA
gptS2 ATGGGTTAAGACAATGACAAAT
a

Engineered restriction endonuclease sites are underlined on the primer sequences.