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Product Introduction
ATTO 488 is a labeling dye with high molecular absorption (90,000) and quantum yield (0.80) as well as sufficient Stokes shift between excitation and emission maximum. It is optimized for excitation with an argon laser, and is characterized by high photostability.ATTO-Dye Labeled PhospholipidsSigma-Aldrich offers a variety of glycero-phospholipids carrying one or two fatty acid groups (lipophilic groups) and a phosphate ester residue (hydrophilic group). They are labeled at the hydrophilic head group. After incorporation of the phospholipid into a membrane the fluorophore is located at the water/lipid interface of the membrane. We currently provide 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine (DPPE), 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE), palmitoyl-sn-glycero-phosphoethanolamine (PPE), and 1,2-dimyristoyl-snglycero-3-phospho-ethanolamine (DMPE) labeled with ATTO-dyes.find more information here
Application
Application
ATTO 488 alkyne is a fluorescent alkyne building block designed for copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) click labeling. The ATTO 488 fluorophore provides bright green emission for fluorescence imaging workflows, while the terminal alkyne enables efficient incorporation into biomolecule conjugates, polymer materials, and surface-functionalized platforms. In practice, this reagent is used to generate fluorescent tags or tracking handles for downstream microscopy, flow cytometry, and fluorescence-based assay development.
1. Biomolecule Click Labeling
ATTO 488 alkyne is used as a fluorescent click handle to label proteins, peptides, and other biomolecules after installing complementary azide functionality. Researchers commonly prepare azide-modified targets (for example, via azide-bearing linkers or azide-functional biomolecule derivatives) and then attach the ATTO 488 alkyne by CuAAC to produce defined fluorescent conjugates for cellular imaging and quantitative fluorescence readouts. The alkyne functionality allows modular assembly of fluorescent probes without requiring dye redesign, which is valuable for building libraries of labeled biomolecules for imaging experiments and fluorescence assay optimization.
2. Fluorescent Probe Construction
ATTO 488 alkyne supports fluorescence probe development where a reactive fluorescent moiety must be introduced into a larger recognition or reporting scaffold. In chemical biology workflows, the alkyne is frequently used to generate fluorescently labeled reporter constructs, such as tagged ligands, multicomponent imaging reagents, or modular FRET-capable assemblies when paired with appropriate complementary fluorophores or quenchers. By enabling post-functionalization through click chemistry, this reagent helps teams rapidly iterate probe architectures and evaluate labeling density and conjugate performance in microscopy and plate-based fluorescence experiments.
3. Surface And Material Functionalization
ATTO 488 alkyne is applied for fluorescent surface engineering and material labeling in biomaterials research and materials characterization. Laboratories often use CuAAC to couple the alkyne-functional dye to azide-bearing coatings, hydrogels, nanoparticles, or polymer films, producing stable fluorescent surfaces that can be tracked during microscopy and imaging studies. This approach is particularly useful when researchers need spatially resolved visualization of functionalized materials, or when they want to compare labeling outcomes across different surface chemistries using the same ATTO 488 reporter.
4. Flow Cytometry Labeling
ATTO 488 alkyne is used to generate green-fluorescent conjugates for flow cytometry workflows where azide-bearing biomolecules or affinity reagents are labeled by click chemistry. After conjugation, the resulting ATTO 488-tagged constructs can be used to quantify binding, uptake, or association in cell populations using standard blue-laser/green-channel instrument configurations. This reagent is also used in reagent development settings to create fluorescent standards or labeling controls for optimizing staining panels and evaluating conjugate performance in fluorescence-based cytometry experiments.
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