Literature DB >> 17985254

Interactive fluorophore and quencher pairs for labeling fluorescent nucleic acid hybridization probes.

Salvatore A E Marras1.   

Abstract

The use of fluorescent nucleic acid hybridization probes that generate a fluorescence signal only when they bind to their target enables real-time monitoring of nucleic acid amplification assays. Real-time nucleic acid amplification assays markedly improves the ability to obtain qualitative and quantitative results. Furthermore, these assays can be carried out in sealed tubes, eliminating carryover contamination. Fluorescent nucleic acid hybridization probes are available in a wide range of different fluorophore and quencher pairs. Multiple hybridization probes, each designed for the detection of a different nucleic acid sequence and each labeled with a differently colored fluorophore, can be added to the same nucleic acid amplification reaction, enabling the development of high-throughput multiplex assays. In order to develop robust, highly sensitive and specific real-time nucleic acid amplification assays it is important to carefully select the fluorophore and quencher labels of hybridization probes. Selection criteria are based on the type of hybridization probe used in the assay, the number of targets to be detected, and the type of apparatus available to perform the assay. This article provides an overview of different aspects of choosing appropriate labels for the different types of fluorescent hybridization probes used with different types of spectrofluorometric thermal cyclers currently available.

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Year:  2007        PMID: 17985254     DOI: 10.1007/s12033-007-9012-9

Source DB:  PubMed          Journal:  Mol Biotechnol        ISSN: 1073-6085            Impact factor:   2.695


  21 in total

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Journal:  Nucleic Acids Res       Date:  2000-01-15       Impact factor: 16.971

2.  Detection of PCR products using self-probing amplicons and fluorescence.

Authors:  D Whitcombe; J Theaker; S P Guy; T Brown; S Little
Journal:  Nat Biotechnol       Date:  1999-08       Impact factor: 54.908

3.  HyBeacon probes: a new tool for DNA sequence detection and allele discrimination.

Authors:  D J French; C L Archard; T Brown; D G McDowell
Journal:  Mol Cell Probes       Date:  2001-12       Impact factor: 2.365

4.  Duplex Scorpion primers in SNP analysis and FRET applications.

Authors:  A Solinas; L J Brown; C McKeen; J M Mellor; J Nicol; N Thelwell; T Brown
Journal:  Nucleic Acids Res       Date:  2001-10-15       Impact factor: 16.971

5.  Efficiencies of fluorescence resonance energy transfer and contact-mediated quenching in oligonucleotide probes.

Authors:  Salvatore A E Marras; Fred Russell Kramer; Sanjay Tyagi
Journal:  Nucleic Acids Res       Date:  2002-11-01       Impact factor: 16.971

6.  Intramolecular dimers: a new strategy to fluorescence quenching in dual-labeled oligonucleotide probes.

Authors:  Mary Katherine Johansson; Henk Fidder; Daren Dick; Ronald M Cook
Journal:  J Am Chem Soc       Date:  2002-06-19       Impact factor: 15.419

Review 7.  Selection of fluorophore and quencher pairs for fluorescent nucleic acid hybridization probes.

Authors:  Salvatore A E Marras
Journal:  Methods Mol Biol       Date:  2006

8.  Continuous fluorescence monitoring of rapid cycle DNA amplification.

Authors:  C T Wittwer; M G Herrmann; A A Moss; R P Rasmussen
Journal:  Biotechniques       Date:  1997-01       Impact factor: 1.993

9.  Kinetic PCR analysis: real-time monitoring of DNA amplification reactions.

Authors:  R Higuchi; C Fockler; G Dollinger; R Watson
Journal:  Biotechnology (N Y)       Date:  1993-09

10.  Oligonucleotides with fluorescent dyes at opposite ends provide a quenched probe system useful for detecting PCR product and nucleic acid hybridization.

Authors:  K J Livak; S J Flood; J Marmaro; W Giusti; K Deetz
Journal:  PCR Methods Appl       Date:  1995-06
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  17 in total

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Journal:  Chemistry       Date:  2009-11-02       Impact factor: 5.236

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5.  Molecular beacons in diagnostics.

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Journal:  F1000 Med Rep       Date:  2012-05-02

6.  Fluorescent-increase kinetics of different fluorescent reporters used for qPCR depend on monitoring chemistry, targeted sequence, type of DNA input and PCR efficiency.

Authors:  Jan M Ruijter; Peter Lorenz; Jari M Tuomi; Michael Hecker; Maurice J B van den Hoff
Journal:  Mikrochim Acta       Date:  2014-01-14       Impact factor: 5.833

7.  Detection and quantification of Lyme spirochetes using sensitive and specific molecular beacon probes.

Authors:  Diana S Saidac; Salvatore A E Marras; Nikhat Parveen
Journal:  BMC Microbiol       Date:  2009-02-24       Impact factor: 3.605

8.  A novel FRET pair for detection of parallel DNA triplexes by the LightCycler.

Authors:  Uffe V Schneider; Jette K Severinsen; Imrich Géci; Limei M Okkels; Nina Jøhnk; Nikolaj D Mikkelsen; Teena Klinge; Erik B Pedersen; Henrik Westh; Gorm Lisby
Journal:  BMC Biotechnol       Date:  2010-01-27       Impact factor: 2.563

9.  A novel multiplex isothermal amplification method for rapid detection and identification of viruses.

Authors:  Dougbeh-Chris Nyan; Kevin L Swinson
Journal:  Sci Rep       Date:  2015-12-08       Impact factor: 4.379

10.  Synthesis and optical properties of pyrrolidinyl peptide nucleic acid carrying a clicked Nile red label.

Authors:  Nattawut Yotapan; Chayan Charoenpakdee; Pawinee Wathanathavorn; Boonsong Ditmangklo; Hans-Achim Wagenknecht; Tirayut Vilaivan
Journal:  Beilstein J Org Chem       Date:  2014-09-11       Impact factor: 2.883

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