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Direct quantification of mRNA expression levels using single molecule detection.

作者信息

Camacho Agnès, Korn Kerstin, Damond Martine, Cajot Jean-François, Litborn Erik, Liao Bohao, Thyberg Per, Winter Holger, Honegger Adrian, Gardellin Paola, Rigler Rudolf

机构信息

Gnothis SA, PSE-B, EPFL, CH-1015 Lausanne, Switzerland.

出版信息

J Biotechnol. 2004 Jan 22;107(2):107-14. doi: 10.1016/j.jbiotec.2003.10.003.

Abstract

Determination of the gene expression by direct quantification of mRNA is becoming increasingly important in basic, pharmaceutical and clinical research. We present a novel approach for gene quantification based on direct hybridization of gene-specific probes to target mRNA sequences in solution at temperatures ensuring absolute specificity of the probe-target complex. No enzymatic steps like reverse transcription or amplification by PCR are involved within the quantification process. In order to increase specificity as well as sensitivity, two probes emitting fluorescence light in different colors are used for our homogeneous assay using fluorescence cross-correlation. We relate to the single molecule sensitivity of excitation and detection in confocal cavities avoiding the amplification of the detected signal. The analysis of the expression level of high, medium and low abundant genes is described in two different cell lines, whereby the genes are quantified in absolute numbers.

摘要

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