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Probe/primer details

ATO291 Tested for in situ hybridization.
Full name
(Alm et al. 1996)
S-*-Ato-0291-a-A-17
Accession no. pB-943
Taxonomy Atopobium; Atopobiaceae; Coriobacteriales; Coriobacteriia; Actinobacteria; Bacteria
Specificity Atopobium cluster
Category animal and human associated microbiota
intestinal microbiota
Target rRNA 16S rRNA
Position 291-307
Sequence 5'- GGT CGG TCT CTC AAC CC -3'
G+C content [%] 65
Length [nt] 17
Check specificity/coverage
Hybridization efficiency
References

Development of 16S rRNA-based probes for the Coriobacterium group and the Atopobium cluster and their application for enumeration of Coriobacteriaceae in human feces from volunteers of different age groups. Harmsen HJ, Wildeboer-Veloo AC, Grijpstra J, Knol J, Degener JE, Welling GW. Applied and environmental microbiology. 2000. Pubmed

Remarks Atopobium cluster includes the Coriobacterium group. No formamide used hybridization temperature 50° C.

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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.