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. 2009 Jun 26;75(17):5445–5450. doi: 10.1128/AEM.00726-09

TABLE 1.

Primers and probe sequences used in this studya

Method and primer or probe Nucleotide sequence (5′-3′)b Reference
Quantitative PCR
    ARC787F ATT AGA TAC CCS BGT AGT CC 27
    ARC915F (FAM)-AGG AAT TGG CGG GGG AGC AC-(TAMRA) 27
    ARC1059R GCC ATG CAC CWC CTC T 27
Nested PCR (DGGE and cloning)
    Ar3F TTC CGG TTG ATC CTG CCG GA 10
    Ar9R CCC GCC AAT TCC TTT AAG TTT C 10
    1492R GGT TAC CTT GTT ACG ACT T 12
    Parch340F-GCc CCC TAC GGG GYG CAS CAG 21
    519R TTA CCG CGG CKG CTG 21
a

All of the primers and DNA probes used in this study were purchased from IDT (Coralville, IA).

b

FAM, 6-carboxyfluorescein; TAMRA, 6-carboxy-tetramethylrhodamine.

c

For DGGE, this primer has the following GC-clamp at the 5′ end: CGCCCGCCGCGCGCGGCGGGCGGGGCGGGGGCACGGGGGG (19).