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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
Chemical Information
Product Specification
Application
Chemical Information
| Purity | ≥80.0% (HPCE) |
Product Specification
| Excitation | 507 |
| Emission | 527 |
| Properties Quality Level | 100 |
| Storage | −20 °C |
Application
ATTO 488 DPPE is a phospholipid-conjugated ATTO 488 fluorophore designed for membrane-associated fluorescent labeling. Its DPPE headgroup enables robust incorporation into lipid bilayers, while the ATTO 488 dye provides bright green fluorescence for microscopy and flow-based readouts. This reagent is commonly used to generate stable fluorescent membranes, vesicles, and supported lipid platforms for imaging and assay development.
1. Liposome Membrane Labeling
ATTO 488 DPPE is frequently used to fluorescently label liposomes and lipid vesicles for visualization of membrane morphology, vesicle trafficking, and membrane mixing experiments in chemical biology and biomaterials research. Researchers incorporate the DPPE lipid into pre-formed lipid mixtures to produce membrane-localized fluorescence that remains associated with the bilayer during handling, enabling consistent tracking of vesicles in fluorescence microscopy and plate-based imaging workflows. The ATTO 488 emission is well matched to standard fluorescence filter sets used for green-channel imaging, making it a practical membrane tracer for studies of lipid composition effects, fusion/aggregation behavior, and vesicle stability under experimental conditions.
2. Supported Lipid Bilayer Imaging
ATTO 488 DPPE is also used to prepare fluorescent supported lipid bilayers (SLBs) and related planar membrane models for microscopy-based characterization of membrane organization and dynamics. By integrating the DPPE lipid into the SLB-forming lipid mixture, researchers obtain a membrane-localized fluorescent signal suitable for monitoring surface-associated processes such as protein adsorption, receptor-ligand binding events, and lateral organization of membrane components. This approach is widely adopted in biophysics and biomaterials laboratories because the dye remains anchored within the membrane, supporting repeated imaging of the same surface region during time-course experiments.
3. Cell Membrane Tracing Assays
ATTO 488 DPPE is commonly applied as a membrane tracer in cell-labeling experiments where a lipid-associated green fluorescence readout is needed for imaging and quantitative assays. Researchers use DPPE-based membrane dyes to mark cell surfaces and/or membrane regions to follow processes such as membrane remodeling, uptake of membrane-associated materials, and cell-to-cell fluorescence transfer in co-culture or interaction studies. The phospholipid nature of ATTO 488 DPPE supports membrane localization rather than diffuse cytosolic labeling, which helps maintain a spatially relevant fluorescence signal for microscopy and flow cytometry workflows that rely on membrane-associated intensity distributions.
4. Nanoparticle Lipid Coating Studies
ATTO 488 DPPE is valuable for fluorescence labeling of lipid-coated nanoparticles and biomimetic carriers where lipid bilayer or lipid-shell presentation is used to mimic biological membranes. In materials science and drug-delivery research, the DPPE lipid component enables incorporation into lipid layers on particle surfaces, allowing researchers to visualize particle association with membranes, quantify surface binding in fluorescence assays, and track particle distribution in imaging experiments. This labeling strategy supports downstream characterization of nanoparticle-membrane interactions using green-channel fluorescence detection, including qualitative microscopy and quantitative fluorescence readouts in multiwell formats.
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