Literature DB >> 20687535

Synthesis and properties of oligonucleotides carrying isoquinoline imidazo[1,2-a]azine fluorescent units.

Sónia Pérez-Rentero1, Nicola Kielland, Montserrat Terrazas, Rodolfo Lavilla, Ramon Eritja.   

Abstract

Oligonucleotides carrying novel fluorescent compounds with a dipolar isoquinoline imidazo[1,2-a]azine core were prepared. Analysis of the melting curves demonstrates that DNA duplexes carrying these fluorescent labels at their ends have a slight increase in DNA duplex stability. The UV absorption and fluorescent properties of the oligonucleotide conjugates were analyzed. The fluorescent label is sensitive to duplex formation, as cooperative melting curves are also observed at 366 nm and fluorescence has a large increase upon denaturation. Cell uptake studies allow observation of these fluorescently labeled oligonucleotides internalized into HeLa cells.

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Year:  2010        PMID: 20687535     DOI: 10.1021/bc1000966

Source DB:  PubMed          Journal:  Bioconjug Chem        ISSN: 1043-1802            Impact factor:   4.774


  1 in total

Review 1.  Modern Synthetic Avenues for the Preparation of Functional Fluorophores.

Authors:  Fabio de Moliner; Nicola Kielland; Rodolfo Lavilla; Marc Vendrell
Journal:  Angew Chem Int Ed Engl       Date:  2017-02-17       Impact factor: 15.336

  1 in total

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