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. 2011 Dec 13;8:534. doi: 10.1186/1743-422X-8-534

Table 1.

Primers used in this study

Primer Sequence (5' - 3') Enzyme site Purpose
P1 GCCAAGCTTAAAACAGCCTGTGGGTTGTTCCCACCC Hind III CV(1-4392) amplification

P2 CGGGTCTAGAGCGTAGACTCTTTTGGCTTCAGTC Xba I CV(1-4392) amplification

P3 CTACGCTCTAGAAAGAAGGA Xba I CV(4381-7410) amplification

P4 ACAAGCGGCCGCTGCTATTCTGGTTATAAC Not I CV(4381-7410) amplification

P5 CTTCTCGAGGTTGATTTTGAGCAAGCATTG Xho I CV(6087-7410-pA) amplification

P6 TATGCGGCCGCTTTTTTTTTTTTTTTTTTTTTTTTT Not I CV(6087-7410-pA) amplification

P7 CTAAAGCTTAGCTAATACGACTCACTATAGTTAAAACAGCCTGTGGGTTG Hind III T7 promoter introduction/priming
cDNA synthesis from negative-strand RNA

P8 CCTATTGCAGACATGATTGACCAG none RT-PCR for negative-strand RNA

P9 TGTTGTTATCTTGTCTCTACTAGTG none RT-PCR for negative-strand RNA

Restriction enzyme sites are underlined