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. 2017 Jan 12;11(1):e0005258. doi: 10.1371/journal.pntd.0005258

Table 1. List of primers and probes used in this study.

Name Length Sequences a Position b
Probe LN34 17 (FAM) AA+C+ACCY+C+T+ACA+A+TGGA (BHQ1) 59–75
Probe LN34a 17 (FAM) AAC+ACCYC+T+ACA+A+TGGA (BHQ1) 59–75
Probe LN34lago 17 (FAM) AA +C +ACTA +C +T +ACA +A +TGGA (BHQ1) 59–75
Probe LN34m 17 (6FAM)-ACACCYCTACAATGGAT-(MGBNFQ) 60–76
Primer forward1 24 ACGCTTAACAACCAGATCAAAGAA 1–24
Primer forward2 25 ACGCTTAACAACAAAATCADAGAAG 1–25
Primer reverse 25 CMGGGTAYTTRTAYTCATAYTGRTC 140–164

a The probes are labeled by fluorescent FAM at the 5′end, Black Hole quencher (BHQ1) at the 3′ end except probe LN34m which is labeled by MGB and NFQ quencher. LNA modified bases are indicated by a plus preceding the base in the sequence (e.g. +A, +G, +C, +T).

b The primer and probe positions are given relative the Lyssavirus full genome (see below).