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. 2012 Jun 1;11:36. doi: 10.1186/1475-2891-11-36

Table 2.

Hybridisation conditions for oligonucleotide probes used in this study

Probe name Sequence (5’ to 3’) Hybridisation pre-treatment Formamide (%) for hybridisation Temperature (°C)
Bacteria covered  
Hybridisation Washing
Ato291
GGTCGGTCTCTCAACCC
Lysozyme
0
50
50
Atopobuim- Coriobacterium
[33]
Bac303
CCAATGTGGGGGACCTT
None
0
46
48
Bacteroides – Prevotella
[34]
Bif164
CATCCGGCATTACCACCC
Lysozyme
0
50
50
Bifidobacterium spp
[35]
Chis150
TTATGCGGTATTAATCTYCCTTT
None
0
50
50
Clostridium histolyticum- Clostridium perfringens
[36]
Erec482
GCTTCTTAGTCARGTACCG
None
0
50
50
Eubacterium rectale- Clostridium coccoides
[36]
Lab158
GGTATTAGCAYCTGTTTCCA
Lysozyme
0
50
50
Lactobacillus- Enterococcus
[37]
Eco1531
CACCGTAGTGCCTCGTCATCA
None
35
37
37
Escherichia coli
[38]
Rrec584
TCAGACTTGCCGYACCGC
None
0
50
50
Roseburia and Eubacterium rectale
[39]
Fprau645
CCTCTGCACTACTCAAGAAAAAC
Lysozyme
15
46
48
Faecalibacterium prausnitzzi
[40]
EUB338‡
GCTGCCTCCCGTAGGAGT
None
35
46
48
Total bacteria 1
[41]
EUB338II‡
GCAGCCACCCGTAGGTGT
None
35
46
48
Total bacteria
[41]
EUB338III‡ GCTGCCACCCGTAGGTGT None 35 46 48 Total bacteria [41]