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Product Introduction
FAM Alkyne is a copper (I)-catalyzed azide-alkyne cycloaddition (CuAAC) reagent of bright green dye used to generate a stable fluorescence signal in bioimaging. The maxima of Ex/Em values are at 494/522 nm, similar to that of Alexa 488 and Cy2. FAM might be excited using 488 nm laser line and displays good optical property. FAM alkyne couples with an azide to form 1,4-disubstituted 1,2,3-triazole inside of living systems without interfering native biochemical processes. Prior to perform CuAAC, the azide functionality should be introduced onto counterpart biomolecule by means of chemical or genetic modification. We offer FAM alkyne as a click chemistry reagent dye for cellular imaging and nucleotide functionalization.
Chemical Information
Product Specification
Application
Chemical Information
| Solubility | DMF, DMSO |
| Appearance | Yellow solid |
Product Specification
| CF280 | 0.18 |
| Excitation | 494 |
| Emission | 522 |
| Storage | -20 °C, protect from light |
Application
FAM Alkyne is a fluorescein (FAM)-based alkyne labeling reagent designed for copper-catalyzed azide-alkyne cycloaddition (CuAAC) workflows. With an alkyne handle for click conjugation and fluorescein's widely used visible emission, this reagent supports fluorescent tagging of biomolecules, affinity reagents, and imaging probes where downstream conjugation is performed under click-compatible conditions.
1. Biomolecule Fluorescent Labeling
FAM Alkyne is used to introduce fluorescein fluorescence into proteins, peptides, and other azide-bearing biomolecules via click chemistry, enabling robust fluorescent labeling for biochemical workflows. Researchers commonly incorporate it into labeling pipelines for binding studies, reagent characterization, and fluorescence readouts in assay development, where the alkyne functionality provides a convenient point of attachment without requiring direct dye conjugation to each target. This format is especially useful when the biological component is first functionalized with an azide group and then fluorescently tagged as a final step for microscopy or plate-based fluorescence measurements.
2. Click-Constructed Fluorescent Probes
FAM Alkyne serves as a fluorescein "reporter" component for building click-assembled fluorescent probes and molecular imaging reagents. In chemical biology and fluorescence probe development, it is frequently coupled to azide-functional targeting ligands, polymers, or scaffold molecules to generate conjugates with defined composition and modular synthesis. The alkyne handle supports stepwise probe construction, allowing teams to screen probe variants by swapping azide-bearing recognition elements while keeping the fluorescein reporting unit consistent for imaging and fluorescence-based characterization.
3. Surface And Material Functionalization
FAM Alkyne is applied in biomaterials research and surface engineering to create fluorescein-functional surfaces and coatings through click conjugation to azide-present substrates. Material scientists and interface-focused labs use it to visualize and quantify surface modification, track immobilized biomolecule layers, or prepare fluorescently labeled polymer systems for microscopy and imaging assays. The click-compatible alkyne functionality supports integration into workflows where surfaces are first prepared with azide groups (or azide-containing linkers) and then reacted with a fluorescein reporter to generate stable, traceable material interfaces.
4. Fluorescence Assay Reagent Development
FAM Alkyne is frequently incorporated into fluorescence assay reagent development where a fluorescein-tagged component is needed for monitoring binding, labeling efficiency, or conjugate formation. Assay developers use the alkyne group to assemble fluorescent reagents from azide-functional partners, supporting standardized construction of fluorescent conjugates used in lab workflows such as reagent QC, fluorescence-based binding experiments, and method optimization. This approach helps teams maintain consistent dye reporting while using click chemistry to control how and where the fluorescent label is installed within the assay construct.
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