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Product Introduction
DusQ1 CPG 500 is a quencher designed for oligonucleotide synthesis and molecular probe applications. It features a non-fluorescent chromophore that efficiently absorbs energy from nearby fluorescent dyes, facilitating fluorescence quenching through Förster Resonance Energy Transfer (FRET) mechanisms. This compound is integrated into solid-phase synthesis workflows, enabling precise control over oligonucleotide labeling and enhancing the development of sophisticated fluorescence-based assays.
Chemical Information
Product Specification
Application
Chemical Information
| Purity | NMR 1H and HPLC-MS (95%) of bound reagent, loading measurement, functional testing in oligo synthesis. |
| Appearance | Purple beads |
Product Specification
| CF260 | 0.17 |
| CF280 | 0.10 |
| Excitation | 522 |
| Storage | Storage: 24 months after receival at -20 °C in the Dark. Transportation: at room temperature for up to 3 weeks. Avoid prolonged exposure to light. Desiccate. |
Application
DusQ1 CPG 500 is a quencher-bearing solid support designed for fluorescence signal suppression in nucleic-acid and fluorescence assay formats. As a click-compatible, conjugation-ready quencher scaffold, it is used to build oligonucleotide-based probes and molecular beacon architectures where proximity-dependent quenching helps reduce background fluorescence prior to target-dependent signal changes. The "CPG 500" format indicates controlled solid-phase presentation, supporting reproducible reagent handling during probe construction workflows.
1. Molecular Beacon Quenching
DusQ1 CPG 500 is used in molecular beacon probe development to create quencher-labeled oligonucleotides that keep fluorescence low in the absence of target. Researchers incorporate this solid-supported quencher into beacon designs where the quencher is positioned to suppress emission from a paired fluorophore until hybridization brings the reporter and quencher into an efficient distance regime. This workflow is common in nucleic-acid assay development for fluorescence readouts using standard plate readers and fluorescence microscopes, where minimizing off-target signal is a practical requirement during optimization.
2. Oligonucleotide Probe Labeling
DusQ1 CPG 500 supports quencher installation into custom oligonucleotide probes used for fluorescence hybridization assays. In typical probe construction workflows, the solid-phase quencher platform enables streamlined incorporation into oligo conjugates used for endpoint fluorescence detection and hybridization monitoring. Molecular biology teams and assay developers rely on quencher-labeled probes to reduce free-dye background and improve the interpretability of fluorescence changes when probes bind complementary sequences in solution or on assay surfaces.
3. FRET-Based Signal Control
DusQ1 CPG 500 is applied in FRET assay engineering where fluorescence suppression is required to establish a clear "off" state before an event generates reporter emission. Teams developing fluorescence-based biosensing reagents use this quencher support to position quenching functionality within oligonucleotide or biomolecule constructs that undergo distance-dependent fluorophore-quencher separation upon binding or processing. The solid support format is particularly useful during reagent prototyping, enabling consistent quencher presentation in multi-component fluorescence systems used for screening and assay optimization.
4. Fluorescent Nucleic Acid Assay Optimization
DusQ1 CPG 500 is frequently used during nucleic acid assay reagent optimization to tune background fluorescence and simplify assay interpretation across different probe architectures. Assay developers use quencher-functionalized solid-phase reagents to iterate probe designs, adjust labeling layouts, and evaluate how quencher placement influences the fluorescence behavior of fluorophore-quencher pairs in hybridization workflows. This application is common in research settings where multiple oligo formats are compared using automated fluorescence instrumentation for rapid optimization of assay conditions.
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