Gene expression analysis using single molecule detection

Recent developments of single molecule detection techniques and in particular the introduction of fluorescence correlation spectroscopy (FCS) led to a number of important applications in biological research. We present a unique approach for the gene expression analysis using dual‐color cross‐correla...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Nucleic acids research 2003-08, Vol.31 (16), p.e89-e89
Hauptverfasser: Korn, Kerstin, Gardellin, Paola, Liao, Bohao, Amacker, Mario, Bergström, Åsa, Björkman, Henrik, Camacho, Agnès, Dörhöfer, Sabine, Dörre, Klaus, Enström, Johanna, Ericson, Thomas, Favez, Tatiana, Gösch, Michael, Honegger, Adrian, Jaccoud, Sandra, Lapczyna, Markus, Litborn, Erik, Thyberg, Per, Winter, Holger, Rigler, Rudolf
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Recent developments of single molecule detection techniques and in particular the introduction of fluorescence correlation spectroscopy (FCS) led to a number of important applications in biological research. We present a unique approach for the gene expression analysis using dual‐color cross‐correlation. The expression assay is based on gene‐specific hybridization of two dye‐labeled DNA probes to a selected target gene. The counting of the dual‐labeled molecules within the solution allows the quantification of the expressed gene copies in absolute numbers. As detection and analysis by FCS can be performed at the level of single molecules, there is no need for any type of amplification. We describe the gene expression assay and present data demonstrating the capacity of this novel technology. In order to prove the gene specificity, we performed experiments with gene‐depleted total cDNA. The biological application was demonstrated by quantifying selected high, medium and low abundant genes in cDNA prepared from HL‐60 cells.
ISSN:0305-1048
1362-4962
1362-4962
DOI:10.1093/nar/gng089