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. 2014 Jan 23;9(1):e86482. doi: 10.1371/journal.pone.0086482

Table 1. Primers used for amplification of NS4A (1–48).

Oligo Sequence (5′-3′)
1 agcctgaccctgaatctgattaccgaaatgggtcgtctgccgacctttatgacccagaaagcacgtgatgcactggataatctgg
2 cagttctgcataccgctgaagccggtggtcgtgcatataatcatgcactgagcgaactgtaag
3 tgctttctgggtcataaaggtcggcagacgacccatttcggtaatcagattcagggtcaggct
4 gatccttacagttcgctcagtgcatgattatatgcacgaccaccggcttcagcggtatgcagaactgccagattatccagtgcatcac
5 ggaggaggatccgaaaacctgtattttcagagcctgaccctgaatctgattaccBamHI
6 ggaggagtcgacctcgagttacagttcgctcagtgcXhoI
7 gcgcgaattcagtacaagcttgctctgaacggEcoRI
8 gctagttattgctcagcgg (T7-Terminator-Primer; Novagen #69337-3)
9 ggaggaccgcggcggtagcctgaccctgaatctgaSacII
10 ggaggagtcgacctcgagttacagttcgctcagtgcSalI
11 gaaattaccgaagagggtcgtctgccgac
12 attcagggtcaggctctgaaaatacaggtt

Note: The sequences of the restriction sites used for cloning are underlined, the name of the enzyme is given below.