Publication | Closed Access
Aminophenyl‐ and Nitrophenyl‐Labeled Nucleoside Triphosphates: Synthesis, Enzymatic Incorporation, and Electrochemical Detection
138
Citations
29
References
2008
Year
Bioorganic ChemistryEngineeringMolecular BiologyOrganic ChemistryEnzymatic ModificationRedox BiologyPrimer ExtensionEnzymatic IncorporationBiosynthesisOn Double StrandNucleic Acid ChemistryOrganic ElectrochemistryElectrochemical DetectionProteomicsBiochemistryOligonucleotideBiomolecular EngineeringCellular EnzymologyNatural SciencesEnzyme CatalysisRedox CurvesNitrophenyl‐labeled Nucleoside
Primer extension is used to incorporate labeled nucleoside triphosphates into oligonucleotides (ONs). Aminophenyl and nitrophenyl modifications serve as electrochemical labels that are detectable by either oxidation or reduction, respectively (see representation of the ON double strand and redox curves). The redox potentials of the labels differ depending on the nucleobase and respond to incorporation into ONs. Supporting information for this article is available on the WWW under http://www.wiley-vch.de/contents/jc_2002/2008/z705088_s.pdf or from the author. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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