
Quasar 670-dT Phosphoramidite
| Catalog Number | A07-0056 |
| Category | RNA/DNA Labeling |
| Molecular Formula | C81H102F6N8O10P2 |
| Molecular Weight | 1523.69 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
Quasar 670 dyes are cyanine derivatives of Cyanine 5. Cyanine dyes are a popular oligonucleotide modification and are commonly used for imaging, flow cytometry, and genomic applications.
Chemical Information
Product Specification
Application
Chemical Information
| Synonyms | 5'-Dimethoxytrityloxy-5-[(N-(6-(N1-ethyl-3,3,3',3'-tetramethylindodicarbocyanin-1'-yl)hexanoyl)-aminohexyl)-3-acrylimido]-2'-deoxyUridine-3'-[(2-cyanoethyl)-(N,N-diisopropyl)]-phosphoramidite, hexafluorophosphate salt |
| IUPAC Name | 2-(5-(1-(6-((6-(3-(1-((2R,4S,5R)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-(((2-cyanoethoxy)(diisopropylamino)phosphaneyl)oxy)tetrahydrofuran-2-yl)-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)acrylamido)hexyl)amino)-6-oxohexyl)-3,3-dimethylindolin-2-ylidene)penta-1,3-dien-1-yl)-1-ethyl-3,3-dimethyl-3H-indol-1-ium;hexafluorophosphate |
| Solubility | Soluble in Anhydrous Acetonitrile |
Product Specification
| Excitation | 647 |
| Emission | 670 |
| Storage | Store at -20 °C |
Application
Quasar 670-dT Phosphoramidite is a fluorescent quencher building block designed for oligonucleotide incorporation, enabling distance-dependent suppression of fluorescence in nucleic-acid probe formats. As a dT phosphoramidite, it integrates directly into DNA during automated solid-phase synthesis, supporting probe architectures where a fluorophore signal is controlled by proximity and conformational changes. This reagent is commonly used in fluorescence-based hybridization assays and molecular beacon-style designs to reduce background and improve readout contrast in nucleic acid analysis workflows.
1. Molecular Beacon Quenching
Quasar 670-dT Phosphoramidite is used to construct molecular beacons and related hairpin probes in which a quencher is positioned to suppress fluorescence when the probe is in its closed state. Researchers incorporate the quencher-bearing nucleotide into the stem region so that target binding opens the structure and spatially separates the fluorophore from the quencher, producing a fluorescence recovery signal. This format is widely adopted in nucleic acid detection studies where real-time optical monitoring is performed using standard fluorescence plate readers or thermocyclers equipped for fluorescence readout.
2. Real-Time Hybridization Probes
Quasar 670-dT Phosphoramidite supports fluorescence hybridization probe development for monitoring nucleic acid targets with controlled background. By placing the quencher within the probe strand (or in a defined internal position for probe variants), assay developers can design constructs that minimize fluorescence from unbound or partially bound states while enabling a stronger signal upon formation of the probe-target duplex. This approach is frequently used in assay optimization for qPCR-like workflows, end-point fluorescence readouts, and multiplex-capable probe sets where quencher placement is tuned to the expected hybridization geometry.
3. FRET-Based Oligonucleotide Assays
Quasar 670-dT Phosphoramidite is also used as an oligonucleotide-compatible quencher component in FRET-based probe systems that rely on efficient donor-quencher proximity control. In these designs, the quencher nucleotide is incorporated into a defined position relative to a fluorophore label so that fluorescence is suppressed in a reference conformation and changes upon target binding, strand displacement, or structural remodeling. Molecular imaging and nucleic acid analytics groups use these constructs to build fluorescence reporting oligos for studying nucleic acid interactions and for developing signal-controlled assay reagents.
4. Genotyping And SNP Assays
Quasar 670-dT Phosphoramidite can be incorporated into oligonucleotide probe designs used for genotyping and single-nucleotide polymorphism discrimination, where fluorescence output depends on the stability of matched versus mismatched duplex formation. Probe developers position the quencher-bearing nucleotide to create a structural or distance-dependent relationship between the fluorophore and quencher that responds to duplex integrity. This enables fluorescence readouts that track hybridization quality in workflows that use fluorescence microscopy, capillary-based optical detection, or plate-based fluorescence instrumentation for nucleic acid characterization.
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