Probe/primer details
| DSR651 | Tested for in situ hybridization. |
| Full name (Alm et al. 1996) |
S-*-Dsb-0651-a-A-18 |
| Accession no. | pB-82 |
| Taxonomy | Desulfobulbaceae; Desulfobacterales; Deltaproteobacteria; delta/epsilon subdivisions; Proteobacteria; Bacteria |
| Specificity | Some Desulfobulbaceae |
| Category | sulfate-reducing microbes |
| Target rRNA | 16S rRNA |
| Position | 651-668 |
| Sequence | 5'- CCC CCT CCA GTA CTC AAG -3' |
| G+C content [%] | 61 |
| Length [nt] | 18 |
| Check specificity/coverage | 
|
| Formamide [%] | 35 |
| Hybridization efficiency |  |
| References | Diversity and vertical distribution of cultured and uncultured Deltaproteobacteria in an intertidal mud flat of the Wadden Sea. Mussmann M, Ishii K, Rabus R, Amann R. Environmental microbiology. 2005. Pubmed Manz W., Eisenbrecher M., Neu T. R. and Szewzyk U. (1998). Abundance and spatial organization of Gram-negative sulfate-reducing bacteria in activated sludge investigated by in situ probing with specific 16S rRNA targeted oligonucleotides. FEMS Microbiol. Ecol. 25: 43-61. |
| Remarks | 70 % FA for CARD-FISH |
| Used in Microarray | SRP-PhyloChip |
Glossary
Name (Alm et al., 1996). Probe designation according to Alm, E. W., Oerther, D. B., Larsen, N., Stahl, D. A., Raskin, L. (1996). The oligonucleotide probe database. Appl Environ Microbiol 62: 3557-9. Abstract (PUBMED).
Position. Probe position according to the E. coli gene numbering.
Sequence. Sequence in IUPAC code: R=G/A, Y=T/C, M=A/C, K=G/T, S=G/C, W=A/T, H=A/C/T, B=G/T/C, V=G/C/A, D=G/A/T, N=G/A/T/C
Tm. Dissoziation temperature according to: Tm=64.9 + 41 x ((G + C - 16.4)/length).
Hybridization efficiency. Use this tool to assess in silico sensitivity (i.e. the hybridization efficiency of the oligonucleotide with its fully complementary target sequence, calculated with ProbeMelt.
Formamide. Percent formamide in the hybridization buffer for optimal hybridization conditions in FISH experiments.
Coverage. Coverage of the three domains calculated using the SILVA reference database 106 if no or a single mismatch is allowed. The detailed method is described in Klindworth et al., 2012. Nucleic Acids Res. 10.1093/nar/gks808 Full Text
Check specificity/coverage. Use these options to reveal the in silico specificity (i.e. number of matching rRNA sequences outside the target taxon) and coverage (i.e. percentage of matching rRNA sequences within the target taxon) of an oligonucleotide against the most recent SSU and LSU rRNA sequence databases.
