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. 2008 Mar;178(3):1615–1622. doi: 10.1534/genetics.107.082164

TABLE 1.

PCR primers used in this study for 16S rRNA gene amplification

Application Name Sequence (5′–3′) Reference
Isolates identification 63F CAGGCCTAACACATGCAAGTCGTT Marchesi et al. (1998)
1492R TACGGYTACCTTGTTACGACTT Lane (1991)
Total community DNA, library construction 8F AGAGTTTGATCMTGGCTCAG
1387R GGGCGGWGTGTACAAGGC
Total community DNA, DGGE analysis 968F GC-Clamp-AACGCGAAGAACCTTAC Heuer et al. (1997)
1378R CGGTGTGTACAAGGCCCGGGAACG
341F (GM5) GC-Clamp-CCTACGGGAGGCAGCAG Muyzer et al. (1993)
907R CCGTCATTCMTTTRAGTTT
GC-Clamp CGCCCGCCGCGCCCCCGCGCCGGTCCCGCCGGCCCCGCCC
Archaeal primers ARCH344F TCGCGCCTGCTGCICCCCGT Giovannoni et al. (1988)
1406R TGYACACACCTCCCGT Olsen et al. (1986)
ARCH519F GWTTTACCGCGGCKGCTG Lane (1991)
ARCH915R GTGCTCTCCCCCGCCAATTC Stahl and Amann (1991)