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Product Introduction
Eclipse® CPG serves as a key component in the realm of oligonucleotide synthesis, featuring a solid support matrix that facilitates efficient nucleotide chain assembly. This product incorporates a controlled pore glass (CPG) substrate, which is chemically modified to enhance the synthesis and labeling of nucleic acids with fluorescent dyes or other functional groups. As a foundational element in the synthesis of labeled oligonucleotides, Eclipse® CPG supports applications in fluorescence-based assays, molecular diagnostics, and nucleic acid research, enabling precise incorporation of reporter molecules for advanced bioimaging and analytical techniques.
Chemical Information
Application
Chemical Information
| Synonyms | 4-N-methyl-N-(4'-nitro-2'-chloroazobenzen-4-yl)-aminobutanamido-1-(2-O-dimethoxytrityloxymethyl)-pyrrolidin-4-yl-succinoyl long chain alkylamino-CPG |
| Appearance | Purple Solid |
Application
Eclipse® CPG is a click-chemistry-compatible solid support designed for preparing functionalized biomolecule and polymer conjugates through efficient surface immobilization and downstream coupling workflows. As a CPG (controlled pore glass) platform, it supports reproducible reagent loading and is frequently used in chemical biology and oligonucleotide/probe construction pipelines where stable attachment and convenient handling are essential. Its practical value is centered on enabling modular synthesis of labeled or functional constructs for fluorescence and binding assays, as well as for building reagent libraries on solid phases.
1. Oligonucleotide Conjugate Assembly
Eclipse® CPG is used in workflows that require attaching functional groups to oligonucleotides or oligonucleotide-derived probes prior to labeling and hybridization experiments. Researchers and assay developers rely on solid-phase handling to standardize reagent loading, simplify wash steps, and produce conjugates that can be carried into downstream fluorescence readouts. In nucleic acid analysis and molecular imaging reagent development, this platform is commonly integrated into probe construction strategies where robust immobilization during intermediate steps improves workflow consistency.
2. Fluorescent Probe Solid-Phase Construction
Eclipse® CPG supports the preparation of fluorescently labeled probes and probe intermediates where modular coupling to a solid support is advantageous. Chemical biology groups use this material to build probe conjugates that can be formatted for microscopy, plate-based fluorescence assays, or other imaging workflows requiring stable reagent handling and straightforward purification. The solid-phase format is particularly helpful when constructing multi-component probe systems, including labeled affinity reagents or reagent libraries used to screen binding or localization performance in fluorescence-based experiments.
3. Biomaterial Surface Functionalization
Eclipse® CPG is applied in biomaterials and materials science settings to generate functionalized surfaces or surface-tethered chemical handles for subsequent bioconjugation. Researchers use the platform to prepare solid-phase reagent materials that can be incorporated into assay formats, affinity capture workflows, or surface-based binding studies where controlled presentation of functional groups is important. This approach is frequently adopted in industrial R&D and translational chemistry platforms that require scalable, reproducible surface modification steps for downstream fluorescent labeling or binding characterization.
4. Click-Enabled Reagent Library Preparation
Eclipse® CPG is leveraged for building click-enabled reagent libraries where many conjugates or labeled intermediates must be prepared with consistent solid-phase processing. In fluorescence chemistry and chemical biology development, teams use the material to generate sets of functionalized constructs for screening reagent performance in assay development and molecular imaging workflows. The controlled pore glass format supports parallel or sequential processing, enabling efficient generation of multiple conjugate variants that can be evaluated by fluorescence readouts in a standardized manner.
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