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. 2008 Oct 7;377(1):221–225. doi: 10.1016/j.bbrc.2008.09.125

Table 1.

Character of each selected epitope and used primers in the design.

Epitope Origin Position(aa) Epitope type Synthesized epitope genes and used primers(5′-3′) in PCRa
F1 S1 24–150 B (neutrallization) S: GTA GGATCCCCACCATGG ATAATTATGTG
A: TCA GGGCCC ATTATAAAATAGA
F2 S1 240–255 B 5′ CAATACTGGTAATTTTTCAGATGGGTTTTACC
CTTTTACTAATTCTAGTGGCGC 3′
F3 S1 290–400 B (neutrallization) S: ACT GGCGCC CAAGGTGGTGTTCA
A: AGT GGGCCC TTCAAAATTTTGTC
F4 S1 532–537 T 5′ CATTAAACTCACTAAAGAGGGT AACGTT GGCGC 3′
F5 S2 1–65 B (neutralization) S: ACT GGCGCC TCTACTAGTGAAAATG
T(CTL) A: AGT GGGCCC ACGTGTTTGTATGTA
F6 N 1–120 T (CTL) S: AGT GGGCCC GCAAGCAGTAAGGCA
B A: ACT GGCGCC ACCCTTAGCAGCA
F7 N 290–410 T (CTL) S: AGT GGCGCC AAGCTTCAACCTGA
A: ACT CTCGAG TTATTAGAGTTCATTTTC
a

Note. Letters in italic means restriction sites, underlined means Kozak sequence, bloded means CpG motif. ‘S′ means sense primer, while ‘A′ means anti-sense primer.