| Literature DB >> 34149274 |
V A Brylev1, I L Lysenko2, E A Kokin1, Y V Martynenko-Makaev2, D Y Ryazantsev1, V V Shmanai2, V A Korshun1,3,4.
Abstract
An azido-derivative of a fluorescein bifluorophore was obtained and used for the synthesis of "molecular beacon"-type oligonucleotide fluorogenic probes for RT-PCR. Eight probe variants were synthesized based on an optimized sequence: with one or two quencher residues at the 3'-end, with a single or bifluorophore fluorescein label attached to 5'-end using modifying phosphoramidites (short linker) or "click reaction" (long linker). Comparison of probes in RT-PCR showed that probes with a doubled quencher (single fluorescein on a short linker) and doubled dye on a short linker (single dye) are somewhat superior in sensitivity to a standard probe (single quencher, single dye on a short linker) by the value of ΔCt = 1-2. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1134/S1068162021030055.Entities:
Keywords: 3,5-diaminobenzoic acid; 5-carboxyfluorescein; fluorescence quenching; fluorogenic DNA probes; real-time qPCR
Year: 2021 PMID: 34149274 PMCID: PMC8193957 DOI: 10.1134/S1068162021030055
Source DB: PubMed Journal: Russ J Bioorg Chem ISSN: 1068-1620 Impact factor: 0.796