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. 2010 Sep 1;48(11):3949–3955. doi: 10.1128/JCM.01256-10

TABLE 2.

Details of primers and probes used in the study

Primer or probe Sequence (5′-3′)a Application Position on genomeb Reference
Primers
    JW12 ATGTAACACC(C/T)CTACAATTG cDNA synthesis, PCR, hnPCR 55-74 9
    JW6 (DPL) CAATTCGCACACATTTTGTG PCR 660-641
    JW6 (E) CAGTTGGCACACATCTTGTG PCR 660-641
    JW6 (M) CAGTTAGCGCACATCTTATG PCR 660-641
    JW10 (DLE2) GTCATCAAAGTGTG(A/G)TGCTC hnPCR 636-617
    JW10 (ME1) GTCATCAATGTGTG(A/G)TGTTC hnPCR 636-617
    JW10 (P) GTCATTAGAGTATGGTGTTC hnPCR 636-617
    001lys ACGCTTAACGAMAAA cDNA synthesis, PCR 1-15 20
    550B GTRCTCCARTTAGCRCACAT PCR, hnPCR 647-666 20
    541lys CACMGSNAAYTAYAARACNAA hnPCR 541-561 This study
    18S rRNA for CGCCGCTAGAGGTGAAATTC Real-time PCR internal control 18S rRNA 23
    18S rRNA rev CGAACC TCCGACTTTCGTTCT Real-time PCR internal control
Probes
    620lyssa FAM-CATCACACCTTGATGACAACTCACAA-BHQ-1 Real-time PCR 620-645 This study
    18S probe FAM-CCGGCGCAAGACGGACCAGA-BHQ-1 Real-time PCR 18S rRNA 23
a

FAM, 6-carboxyfluorescein; BHQ-1, Black Hole Quencher 1.

b

Nucleotide positions are numbered according to the Pasteur virus sequence (GenBank accession number M13215).