Literature DB >> 15490558

The effect of nucleobase-specific fluorescence quenching on in situ hybridization with rRNA-targeted oligonucleotide probes.

Sebastian Behrens1, Bernhard M Fuchs, Rudolf Amann.   

Abstract

Oligonucleotide probes labeled with fluorescent dyes are used in a variety of in situ applications to detect specific DNA or RNA molecules. It has been described that probe fluorescence might be quenched upon hybridization in a sequence specific way. Here, a set of 17 oligonuleotides labeled with 6-carboxyfluorescein was used to examine the relevance of nucleotide specific quenching for fluorescence in situ hybridization (FISH) to whole fixed bacterial cells. Probes quenched upon hybridization to a guanine-rich region of purified RNA in solution were not quenched upon FISH. Among other factors the high protein concentration within cells may prevent quenching of probe fluorescence in situ.

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Year:  2004        PMID: 15490558     DOI: 10.1078/0723202041748136

Source DB:  PubMed          Journal:  Syst Appl Microbiol        ISSN: 0723-2020            Impact factor:   4.022


  3 in total

1.  Making all parts of the 16S rRNA of Escherichia coli accessible in situ to single DNA oligonucleotides.

Authors:  L Safak Yilmaz; Hatice E Okten; Daniel R Noguera
Journal:  Appl Environ Microbiol       Date:  2006-01       Impact factor: 4.792

2.  Wavelength dependant quenching of 2,5-diphenyloxazole fluorescence by nucleotides.

Authors:  N V Krishnamurthy; A R Reddy; B Bhudevi
Journal:  J Fluoresc       Date:  2007-09-03       Impact factor: 2.217

3.  T7 RNA polymerase non-specifically transcribes and induces disassembly of DNA nanostructures.

Authors:  Samuel W Schaffter; Leopold N Green; Joanna Schneider; Hari K K Subramanian; Rebecca Schulman; Elisa Franco
Journal:  Nucleic Acids Res       Date:  2018-06-01       Impact factor: 16.971

  3 in total

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