| EUB338 II (SBACT P 338) | Tested for in situ hybridization. |
| Full name (Alm et al. 1996) |
S-*-BactP-0338-a-A-18 |
| Accession no. | pB-160 |
| Taxonomy | Planctomycetales [1]; Planctomycetia [1]; Planctomycetes [1]; Bacteria [1] |
| Specificity | Planctomycetales |
| Category | higher taxonomic levels [1] |
| Target rRNA | 16S rRNA |
| Modified version(s) | EUB338 (Bact338) (bacterial) [1] EUB338 III (SBACT V 338) [1] |
| Position | 338-355 |
| Sequence | 5'- GCA GCC ACC CGT AGG TGT -3' |
| G+C content [%] | 67 |
| Length [nt] | 18 |
| Check specificity/coverage |  [2]
|
| Formamide [%] | 0-50 |
| Hybridization efficiency |  [2] |
| References | The domain-specific probe EUB338 is insufficient for the detection of all Bacteria: development and evaluation of a more comprehensive probe set. Daims H, Brühl A, Amann R, Schleifer KH, Wagner M. Systematic and applied microbiology. 1999. Pubmed [2] |
| Remarks | Use probe in equimolar mixture together with probes EUB338 and EUB338III to detect all bacteria. |
| Used in Microarray | SRP-PhyloChip [1] RHC-PhyloChip [1] Freshwater Sediment-Microarray [1] Burkholderia-Phylochip [1] |
Print [1]
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) [2].
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 [2].
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 [2]
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.