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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) |
| NACRES | NA.32 |
Product Specification
| Excitation | 507 |
| Emission | 527 |
| Properties Quality Level | 100 |
| Storage | −20 °C |
Application
ATTO 488 DMPE is a fluorescent dye built on an ATTO 488 chromophore combined with a DMPE lipid anchor, enabling robust incorporation into lipid environments and membrane-associated labeling formats. Its excitation and emission are centered in the green spectral region, making it a widely used reporter for fluorescence microscopy workflows and fluorescence-based assay development where lipid-context labeling is required. The DMPE functionality supports stable association with phospholipid bilayers, supporting visualization of membrane features and preparation of fluorescent lipid conjugates for imaging and analytical studies.
1. Membrane Labeling Microscopy
ATTO 488 DMPE is commonly used to label cell membranes and membrane-mimicking systems for fluorescence microscopy, including studies of membrane organization, trafficking-related membrane remodeling, and membrane-associated binding events. Researchers incorporate the DMPE-lipid anchor into supported lipid bilayers, liposomes, or cell membrane preparations to generate a stable green fluorescent membrane signal that can be imaged on standard epifluorescence and confocal platforms using appropriate green-channel filter sets. This reagent is frequently selected when a lipid-localized fluorophore is preferred over covalent protein labeling, enabling visualization of membrane dynamics without requiring a specific protein target.
2. Liposome And Nanovesicle Tracing
ATTO 488 DMPE supports fluorescence labeling of liposomes and other lipid-based nanovesicles used in delivery, uptake, and interaction studies. By anchoring the dye to lipid membranes, it enables tracking of vesicle association with cells or model membranes and monitoring vesicle stability in fluorescence readouts. In typical workflows, ATTO 488 DMPE-labeled vesicles are used as imaging reagents to follow vesicle binding and internalization in microscopy experiments, and as fluorescent tracers in plate-based assays where vesicle-membrane interactions are quantified by green fluorescence intensity.
3. Flow Cytometry Membrane Dyes
ATTO 488 DMPE is used as a membrane-associated fluorescence reagent in flow cytometry workflows where green fluorescence reporting of cell surface or membrane labeling is needed. The DMPE anchor helps maintain dye localization within lipid membranes during sample handling, supporting consistent signal for population-level analysis. Researchers often employ ATTO 488 DMPE in multicolor panels by selecting appropriate excitation/emission channels for ATTO 488 and using spectral compensation strategies consistent with green fluorophores. This approach is particularly useful for experiments that require labeling based on membrane context rather than targeting a specific membrane protein.
4. Fluorescent Lipid Standards
ATTO 488 DMPE is also used to prepare fluorescent lipid standards and reference materials for method development and instrument verification in fluorescence-based lipid assays. In laboratories developing membrane or liposome quantification protocols, the dye provides a convenient green fluorescent signal tied to a lipid anchor, enabling reproducible calibration of fluorescence responses across experiments. Teams performing assay optimization for lipid mixing, vesicle binding, or membrane incorporation studies may use ATTO 488 DMPE as a consistent reference reagent to validate assay setup and compare fluorescence outputs between runs.
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