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Publisert 2003

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Publikasjonsdetaljer

Tidsskrift : Nucleic Acids Research (NAR) , vol. 31 , p. e117 , 2003

Utgiver : Oxford University Press

Internasjonale standardnummer :
Trykt : 0305-1048
Elektronisk : 1362-4962

Publikasjonstype : Vitenskapelig artikkel

Bidragsytere : Rudi, Knut; Holck, Askild Lorentz

Har du spørsmål om noe vedrørende publikasjonen, kan du kontakte Nofimas bibliotekleder.

Kjetil Aune
Bibliotekleder
kjetil.aune@nofima.no

Sammendrag

Quencher extension (QEXT) is a novel single step closed tube real-time method to quantify SNPs using reporters and quenchers in combination with primer extension. A probe with a 5'-reporter dye is single base extended with a dideoxy nucleotide containing a quencher dye if the target SNP allele is present. The extension is recorded from the quenching (reduced fluorescence) of the reporter dye. This avoids the influence from the unincorporated dye-labeled nucleotides, resulting in high accuracy and signal to noise ratio. The relative amount of a specific SNP allele is determined from the nucleotide incorporation rate in a thermo-cycling reaction. We tested the QEXT assay using five SNPs in the Listeria monocytogenes inlA gene as a model system. The presence or the target SNP alleles were determined with high statistical confidence (p < 0.0005).The quantitative detection limits were between 0 and 5 % for the targeted SNP alleles in a background of other SNP alleles (p < 0.05). The QEXT method is directly adaptable to current real-time PCR equipment, and is thus suited for high-throughput and a wide application range.

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