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. 2018 May 16;15:38. doi: 10.1186/s12977-018-0419-0

Table 2.

Primers used for cloning and PCR detection

Primer name Sequence (5′–3′)
pCF7-Vif cloning
FFV-Vif #1 GCGGGCTAGCGCCGCGGTACACACCGTCAAAGCCATGAGCGAGGGGACTGGCAG
FFV-Vif #2 GTGCTCTCCAAAGACCGGTTATCACAGCTCGCCGCTCCACAGCAGATTCC
FFV-Vif #3 GGCGAGCTGTGATAACCGGTCTTTGGAGAGCACAAGCTGATG
FFV-Vif #4 CGCTCTGTTGCATGCCG
Mutagenesis of the upstream start codon
FFV 9233-F GCGGTCCGGAACACCCAAGACGGATCCTACTCG
M/T-R CGGCGCTAGCTCTAGTTAGCGTAGTCAAATCCCTCTCCCCAC
M+-R CGGCGCTAGCTCTAGTTACCATAGTGAAATCCCTCTCCCCAC
PCR amplification of in vitro-selected FFV-Vif variants
FFV 9366-F CCACTTCTGTTTGGACCTTACC
FFV-10288-R CAGCTTGTGCTCTCCAAAGC
Nested FFV PCR
FFVgag-F1 CTACAGCCGCTATTGAAGGAG
FFVgag-R1 CCCTGCTGTTGAGGATTACC
FFVgag-F2 TTACAGATGGAAACTGGTCCTTAGT
FFVgag-R2 CATCAGAGTGTTGCTGTTGTTG
Real-time quantitative PCR
FFVgag -F GGACGATCTCAACAAGGTCAACTAAA
FFVgag-R TCCACGAGGAGGTTGCGA
FFVgag-TM AGACCCCCTAGACAACAACAGCAACACT