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Probe/primer details

Aalborgi183 Tested for in situ hybridization.
Full name
(Alm et al. 1996)
S-S-B.aalborgi-0183-a-A
Accession no. pB-3932
Taxonomy Brachyspira aalborgi; Brachyspira; Brachyspiraceae; Brachyspirales; Spirochaetia; Spirochaetes; Bacteria
Specificity Brachyspira aalborgi cluster 1
Category animal and human associated microbiota
intestinal microbiota
Target rRNA 16S rRNA
Position 183-200
Sequence 5'- CTA CGC TTT AGC GTC AAG -3'
G+C content [%] 50
Length [nt] 18
Check specificity/coverage
Hybridization efficiency
References

Diagnostic examination of human intestinal spirochetosis by fluorescent in situ hybridization for Brachyspira aalborgi, Brachyspira pilosicoli, and other species of the genus Brachyspira (Serpulina). Jensen TK, Boye M, Ahrens P, Korsager B, Teglbjaerg PS, Lindboe CF, Møller K. Journal of clinical microbiology. 2001. Pubmed

Remarks No formamide used hybridization and washing temperature: 37° 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.