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Product Introduction
ATTO 594 is a fluorescent label belonging to the class of Rhodamine dyes. The dye is designed for application in the area of life science, e.g. labeling of DNA, RNA or proteins. Characteristic features of the label are strong absorption, high fluorescence quantum yield, high thermal and photo-stability, excellent water solubility, and very little triplet formation. After coupling to a substrate ATTO 594 carries a net electrical charge of -1.ATTO-Dye Labeled Phospholipids Sigma-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-sn-glycero-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 | 600 |
| Emission | 629 ±5 |
| Properties Quality Level | 100 |
| Storage | −20 °C |
Application
ATTO 594 DPPE is a lipophilic ATTO 594 fluorescent dye conjugated to DPPE, enabling stable incorporation into phospholipid membranes and membrane-mimetic systems. This amphiphilic construct is widely used as a bright, photostable membrane label for fluorescence microscopy and flow-based readouts, where the dye's red emission supports multicolor imaging with appropriate filter sets.
1. Membrane Labeling
ATTO 594 DPPE is used to fluorescently label lipid bilayers in supported lipid bilayers, liposomes, and cell-derived membrane preparations for visualization of membrane structure and dynamics. Researchers incorporate the dye-lipid into lipid mixtures prior to vesicle formation or bilayer assembly, then image the resulting membrane systems by confocal or widefield fluorescence microscopy. Because the dye is tethered to a phospholipid (DPPE), the label remains associated with the membrane phase during typical imaging and washing steps, supporting studies of lipid organization, membrane remodeling, and membrane-associated interactions.
2. Liposome Tracking Studies
ATTO 594 DPPE supports fluorescence-based tracking of liposomes in assays where membrane integrity and trafficking-like behavior are monitored under controlled experimental conditions. In materials and chemical biology workflows, the labeled vesicles are used to follow binding to model surfaces, adsorption to biomaterial coatings, or uptake-like behavior in simplified in vitro systems. The red fluorescence output is particularly convenient for separating liposome signal from background autofluorescence and for combining with additional probes in multichannel experiments when spectral overlap is managed through instrument settings and controls.
3. Flow Cytometry Membrane Probing
ATTO 594 DPPE is applied as a membrane stain for flow cytometry to quantify fluorescence associated with cell surfaces or membrane-enriched particles after membrane-associated labeling. In cell biology and biomaterials screening, the reagent is used to generate a robust fluorescent signal that reports on membrane labeling levels across populations, enabling gating and comparative analysis between experimental conditions. The DPPE lipid anchor helps maintain dye association with membranes during staining and measurement workflows, supporting reproducible cytometric readouts for membrane-related experiments.
4. Multicolor Imaging Reagent
ATTO 594 DPPE is frequently selected as a red-emitting membrane fluorophore for multicolor fluorescence imaging experiments that require a membrane-resident label alongside other fluorescent markers. Imaging teams use it to create spectral separation between membrane labeling and co-stained targets such as proteins, nucleic acids, or cytoskeletal components, using sequential acquisition or appropriate filter configurations. This makes ATTO 594 DPPE a practical component in fluorescence panel development for microscopy studies focused on spatial relationships between membranes and biomolecular components.
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