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. 2013 Dec 3;4:359. doi: 10.3389/fmicb.2013.00359

Table 2.

Overview of the used primers in this study.

Oligo. namea Target Oligo. sequence (5'–3') Positionb GC (%) Tm Amplicon size Assay References
ARC 109-F Archaea 16S rRNA gene ACK GCT CAG TAA CAC GT 109–125 47 54 826 TRFLP sequencing Großkopf et al., 1998
ARC 934-R GTG CTC CCC CGC CAA TTC CT 915–934 65 71
CYA 359_mod-F Cyanobacteria 16S rRNA gene GRG GAA TYT TCC GCA ATG GG 359–378 60 63 447 qPCR Nuebel et al., 1997
CYA 781-R GAC TAC WGG GGT ATC TAA TCC CWT T 791–805 46 64
mlas-mod-F Universal mcrA gene GGY GGT GTM GGD TTC ACM CAR TA 976–998a 43–65 68 469 qPCR Steinberg and Regan, 2008
mcrA-rev-R CGT TCA TBG CGT AGT TVG GRT AGT 1421–1444a 42–54 66
a

F, forward primer; R, reverse primer.

b

Positions are based on the following: primers targeting the 16S rRNA gene—E.coli; primers targeting the mcrA gene—M. thermautotrophicus mcrA gene accession number: U10036 (following Steinberg and Regan, 2008).