Double labeling of oligonucleotide probes for fluorescence in situ hybridization (DOPE-FISH) improves signal intensity and increases rRNA accessibility.
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Invasive Harlequin Ladybird Carries Biological Weapons Against Native CompetitorsScanning a microhabitat: plant-microbe interactions revealed by confocal laser microscopy.Ecophysiology of an uncultivated lineage of Aigarchaeota from an oxic, hot spring filamentous 'streamer' community.MiL-FISH: Multilabeled Oligonucleotides for Fluorescence In Situ Hybridization Improve Visualization of Bacterial Cells.Genomic insights into members of the candidate phylum Hyd24-12 common in mesophilic anaerobic digestersA Novel Extracellular Gut Symbiont in the Marine Worm Priapulus caudatus (Priapulida) Reveals an Alphaproteobacterial Symbiont Clade of the EcdysozoaIn situ visualization of newly synthesized proteins in environmental microbes using amino acid tagging and click chemistry.Molecular characterization of putative biocorroding microbiota with a novel niche detection of Epsilon- and Zetaproteobacteria in Pacific Ocean coastal seawaters.Metatranscriptomics of the marine sponge Geodia barretti: tackling phylogeny and function of its microbial community.A straightforward DOPE (double labeling of oligonucleotide probes)-FISH (fluorescence in situ hybridization) method for simultaneous multicolor detection of six microbial populations.Strong inter-population cooperation leads to partner intermixing in microbial communities.Microbial life associated with low-temperature alteration of ultramafic rocks in the Leka ophiolite complex.Multiple single-cell genomes provide insight into functions of uncultured Deltaproteobacteria in the human oral cavity.Biofilm growth mode promotes maximum carrying capacity and community stability during product inhibition syntrophyFunctionally relevant diversity of closely related Nitrospira in activated sludge.Tracking heavy water (D2O) incorporation for identifying and sorting active microbial cells.Sequentially aerated membrane biofilm reactors for autotrophic nitrogen removal: microbial community composition and dynamicsMolecular biology-based methods for quantification of bacteria in mixed culture: perspectives and limitations.Cultivation of an obligate acidophilic ammonia oxidizer from a nitrifying acid soil.Fluorescence in situ hybridization and sequential catalyzed reporter deposition (2C-FISH) for the flow cytometric sorting of freshwater ultramicrobacteria.Direct visualization of the novel pathogen, Spiroplasma eriocheiris, in the freshwater crayfish Procambarus clarkii (Girard) using fluorescence in situ hybridization.Identification of active denitrifiers in full-scale nutrient removal wastewater treatment systems.Characterization of the In Situ Ecophysiology of Novel Phylotypes in Nutrient Removal Activated Sludge Treatment PlantsEfficient enzymatic synthesis and dual-colour fluorescent labelling of DNA probes using long chain azido-dUTP and BCN dyesTrace incorporation of heavy water reveals slow and heterogeneous pathogen growth rates in cystic fibrosis sputum.Isolation of 'Candidatus Nitrosocosmicus franklandus', a novel ureolytic soil archaeal ammonia oxidiser with tolerance to high ammonia concentration.Fluctuations in butyrate-producing bacteria in ulcerative colitis patients of North IndiaVisualizing in situ translational activity for identifying and sorting slow-growing archaeal-bacterial consortia.Functional single-cell analyses: flow cytometry and cell sorting of microbial populations and communities.It is all about location: how to pinpoint microorganisms and their functions in multispecies biofilms.Culture-Independent Analyses Reveal Novel Anaerolineaceae as Abundant Primary Fermenters in Anaerobic Digesters Treating Waste Activated Sludge.Fluorescence in situ hybridization (FISH) in the microbiological diagnostic routine laboratory: a review.Critical review on biofilm methods.Ammonia-oxidizing archaea as main drivers of nitrification in cold-water sponges.New methods for analysis of spatial distribution and coaggregation of microbial populations in complex biofilms.Fluorescence In Situ Hybridization for Diagnosis of Whipple's Disease in Formalin-Fixed Paraffin-Embedded Tissue.Single-Cell Growth Rates in Photoautotrophic Populations Measured by Stable Isotope Probing and Resonance Raman Microspectrometry.Genomic and in situ investigations of the novel uncultured Chloroflexi associated with 0092 morphotype filamentous bulking in activated sludgeMicrobiology of folliculitis: a histological study of 39 cases.Fluorescent labeling agents for quorum-sensing receptors (FLAQS) in live cells.
P2860
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P2860
Double labeling of oligonucleotide probes for fluorescence in situ hybridization (DOPE-FISH) improves signal intensity and increases rRNA accessibility.
description
2009 nî lūn-bûn
@nan
2009 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Double labeling of oligonucleo ...... increases rRNA accessibility.
@ast
Double labeling of oligonucleo ...... increases rRNA accessibility.
@en
type
label
Double labeling of oligonucleo ...... increases rRNA accessibility.
@ast
Double labeling of oligonucleo ...... increases rRNA accessibility.
@en
prefLabel
Double labeling of oligonucleo ...... increases rRNA accessibility.
@ast
Double labeling of oligonucleo ...... increases rRNA accessibility.
@en
P2860
P50
P356
P1476
Double labeling of oligonucleo ...... increases rRNA accessibility.
@en
P2093
Christiane Dorninger
P2860
P304
P356
10.1128/AEM.02456-09
P407
P577
2009-12-04T00:00:00Z