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. 2013 Oct 28;2013:594319. doi: 10.1155/2013/594319

Table 1.

Primers used for cloning N gene domains of CHPV.

S. no. Construct Oligo name Primer sequence
1 BD-N1 and AD-N1 N1 F NdeI (BD/AD) GGAAGTGACATATGAGTTCTCAAGTATTCTGC
N1 R BamHI (BD/AD) GCTAACAGGATCCGAAGAATGCCCCTGGAAAC
2 BD-N2 and AD-N2 N2 F NdeI (BD/AD) GGAAGTGACATATGGAAGACCCAGTGGAGTTTC
N2 R BamHI (BD/AD) GCTAACAGGATCCATGGAAACTGGGATTTTTTGTTG
3 BD-N3 and AD-N3 N3 F NdeI (BD/AD) GGAAGTGACATATGACTCTGTCACACCTCCAG
N3 R BamHI (BD/AD) GCTAACAGGATCCTCATGCAAAGAGTTTCCTGGC
4 GST-N1 N1 F BamHI (pGEX-4T3) GCTAACAGGATCCATGAGTTCTCAAGTATTCTGC
N1 R XhoI (pGEX-4T3) GCTAACACTCGAGGAAGAATGCCCCTGGAAAC
5 GST-N2 N2 F BamHI (pGEX-4T3) GCTAACAGGATCCATGGAAGACCCAGTGGAGTTTC
N2 R XhoI (pGEX-4T3) GCTAACACTCGAGATGGAAACTGGGATTTTTTGTTG
6 GST-N3 N3 F BamHI (pGEX-4T3) GCTAACAGGATCCATGACTCTGTCACACCTCCAG
N3 R XhoI (pGEX-4T3) GCTAACACTCGAGTCATGCAAAGAGTTTCCTGGC

Primers used for PCR amplification of Chandipura Virus N1, N2, and N3 domains of nucleocapsid gene (F: forward primer and R: reverse primer). The names of the restriction enzymes are in italics and their recognition sequences in bold.