| Literature DB >> 14711494 |
Agnès Camacho1, Kerstin Korn, Martine Damond, Jean-François Cajot, Erik Litborn, Bohao Liao, Per Thyberg, Holger Winter, Adrian Honegger, Paola Gardellin, Rudolf Rigler.
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.Mesh:
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Year: 2004 PMID: 14711494 DOI: 10.1016/j.jbiotec.2003.10.003
Source DB: PubMed Journal: J Biotechnol ISSN: 0168-1656 Impact factor: 3.307