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. 2009 Nov 20;76(2):536–545. doi: 10.1128/AEM.01797-09

TABLE 2.

Primers and probes used for real-time RT-PCR in this study

Primer or probe Typee Sequencef Position
NLV-RT-FWDaa NV, sense primer TGT TYA GRT GGA TGA GRT TCT C 5013-5034g
COG2Rb NV, antisense primer TCG ACG CCA TCT TCA TTC ACA 5100-5079h
QNIFS-BHQc NV, probe FAM-AGC ACG TGG GAG GGC GAT CG-BHQ1 5042-5061h
MS2-TM2-Fd MS2, sense primer TGC TCG CGG ATA CCC G 3169-3184i
MS2-TM2-Rd MS2, antisense primer AAC TTG CGT TCT CGA GCG AT 3229-3210i
MS2-TM2JOEd MS2, probe JOE-ACC TCG GGT TTC CGT CTT GCT CGT-BHQ1 3186-3209i
a

Modified sequence QNIF2 as described by Loisy et al. (61).

b

Data from reference 49.

c

Sequence QNIFS as described by Loisy et al. (61) modified with quencher dye BHQ1 at the 3′ end.

d

Data from reference 29.

e

NV, norovirus detection; MS2, MS2 detection.

f

Y = C or T; R = A or G; FAM, 6-carboxyfluorescein; BHQ1, black hole quencher 1; JOE, 6-carboxy-4′,5′ -dichloro-2′,7′-dimethoxyfluorescein.

g

Position in the nucleotide sequence of Lordsdale virus (GenBank accession no. X86557).

h

Position in the nucleotide sequence of Camberwell virus (accession no. AF145896).

i

Position in the nucleotide sequence of phage MS2 (accession no. V00642).