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Product Introduction
ATTO 490LS is a new fluorescent label featuring an extraordinary large Stokes-Shift of 165 nm. Thus the emission spectrum is almost completely separated from its absorption spectrum, making the dye highly suitable for multiplexing experiments, in particular in combination with ATTO 488 and ATTO 514. ATTO 490LS is very hydrophillic and shows excellent water solubility. The dye exhibits a relatively high fluorescence quantum yield, which is only slightly reduced after conjugation to biomolecules, e.g. proteins, even at high degrees of labeling (DOL). ATTO 490LS is an anionic dye. After conjugation to a substrate the dye carries a net electrical charge of -1.The azide modification is used in the Huisgen reaction (“Click Chemistry“).find more information here
Chemical Information
Application
Chemical Information
| NACRES | NA.32 |
Application
ATTO 490LS azide is a fluorescent azide building block used to introduce an ATTO 490LS dye handle into biomolecules and materials via azide-based click chemistry. Its azide functionality enables efficient bioorthogonal conjugation workflows, while the ATTO 490LS fluorophore supports fluorescence-based visualization and quantification in labeling and imaging experiments. Researchers use this reagent to construct fluorescent conjugates for tracking, microscopy, and assay development where a robust, dye-defined labeling step is required.
1. Biomolecule Labeling
ATTO 490LS azide is widely used by chemical biology and glycobiology groups to label proteins, peptides, and other biomolecule scaffolds that have been equipped with complementary click partners (commonly strained alkynes or cyclooctynes). In practice, the azide provides a convenient fluorescent tag for downstream fluorescence microscopy and fluorescence readouts, including experiments that require controlled dye stoichiometry and modular conjugate construction. This reagent is also frequently incorporated into labeling strategies for affinity reagents and multicomponent probes where the fluorophore must be installed through a selective conjugation step rather than nonspecific dye coupling.
2. Fluorescent Probe Construction
ATTO 490LS azide supports fluorescent probe development for researchers building modular imaging reagents, including nucleic-acid-associated and peptide-based probe formats that rely on click-compatible conjugation. By installing the ATTO 490LS fluorophore through the azide handle, probe developers can generate labeled constructs for localization studies, binding assays, or fluorescence-based reporting platforms that benefit from a defined attachment point. The click-compatible nature of the reagent is particularly useful when probe assembly must be compatible with sensitive biomolecules or when multiple functional elements need to be introduced in a stepwise workflow.
3. Surface And Polymer Functionalization
ATTO 490LS azide is used in biomaterials and materials chemistry workflows to create fluorescently addressable surfaces and polymer coatings through azide-enabled click attachment to surface-presented or tethered click partners. This approach is common in studies that visualize material interfaces, track biomolecule adsorption, or generate fluorescently labeled hydrogels and coatings for microscopy-based characterization. In these applications, the dye's incorporation via a click handle helps maintain labeling consistency across batches and supports reproducible fluorescence imaging of functionalized materials.
4. Imaging And Flow Cytometry Tracing
ATTO 490LS azide is employed as a fluorescence labeling reagent for cellular and biochemical tracing experiments where azide-based click conjugation is used to install the fluorophore onto targeting or recognition components prior to imaging or analysis. Laboratories use the resulting fluorescent conjugates for microscopy-based localization and for flow cytometry workflows that require a fluorescent tag introduced through a defined conjugation step. This is especially relevant in experimental designs where researchers want to minimize background from nonspecific labeling and rely on click-installed fluorescence to report on binding or association events in complex samples.
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