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Probe/primer details

G123T Tested for in situ hybridization.
Full name
(Alm et al. 1996)
S-G-Thioth-697-a-A-18
Accession no. pB-170
Taxonomy Thiothrix; Thiotrichaceae; Thiotrichales; Gammaproteobacteria; Proteobacteria; Bacteria
Specificity Thiothrix eikelboomii, T. nivea, T. unzii, T. fructosivorans, T. defluvii, Eikelboom type 021N group I, II, III
Category S-oxidizing (sulfur-oxidizing) bacteria
bacteria of relevance in wastewater treatment
Competitor 5'-CCT TCC GAT CTC TAC GCA -3'
Target rRNA 16S rRNA
Position 697-714
Sequence 5'- CCT TCC GAT CTC TAT GCA -3'
G+C content [%] 50
Length [nt] 18
Check specificity/coverage
Formamide [%] 40
Hybridization efficiency
References

Phylogenetic analysis of and oligonucleotide probe development for eikelboom type 021N filamentous bacteria isolated from bulking activated sludge. Kanagawa T, Kamagata Y, Aruga S, Kohno T, Horn M, Wagner M. Applied and environmental microbiology. 2000. Pubmed

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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.