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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 | ≥90.0% (HPCE) |
| NACRES | NA.32 |
Product Specification
| Excitation | 600 |
| Emission | 629 ±5 |
| Properties Quality Level | 100 |
| Storage | −20 °C |
Application
ATTO 594 DMPE is a red-emitting ATTO 594 dye delivered as a DMPE (1,2-dimyristoyl-sn-glycero-3-phosphoethanolamine) lipid conjugate, enabling efficient incorporation into lipid membranes and lipid-based materials. Its strong fluorescence in the visible range makes it a widely used molecular label for membrane-associated studies where robust, dye-based contrast is required. Researchers frequently use this reagent to generate membrane stains and fluorescent lipid probes for imaging and flow-based readouts.
1. Lipid Membrane Labeling
ATTO 594 DMPE is used to fluorescently label cell membranes and model lipid bilayers by incorporating the dye-lipid into phospholipid environments. In membrane staining workflows, it supports visualization of membrane distribution and membrane-associated processes in microscopy experiments, including studies of membrane remodeling, vesicle formation, and lipid mixing assays. Because the dye is presented on a phosphoethanolamine lipid anchor, it is commonly selected for experiments that require a stable association with lipid phases rather than nonspecific protein labeling.
2. Vesicle And Liposome Imaging
ATTO 594 DMPE is frequently incorporated into liposomes and extracellular vesicle (EV)-mimicking lipid vesicles to enable tracking of vesicle localization, trafficking, and uptake in fluorescence microscopy. In vesicle characterization workflows, it provides a convenient fluorescent handle for comparing vesicle populations, monitoring vesicle integrity during handling, and visualizing vesicle interactions with membranes or biomaterials. This reagent is also used in assay development settings where membrane-bound fluorescence is needed to follow vesicle behavior over time.
3. Flow Cytometry Membrane Staining
ATTO 594 DMPE is applied as a fluorescence-labeling reagent for flow cytometry-based analysis of membrane-associated signals, particularly when the experimental readout depends on lipid membrane incorporation rather than covalent biomolecule conjugation. Researchers use it to stain membrane-containing particles and cells to quantify fluorescence intensity distributions and compare labeling across experimental conditions. In multiplex fluorescence panels, it is typically chosen for its red emission contribution when instrument filter sets are configured for ATTO 594-compatible channels.
4. Biomaterial Surface Fluorescent Probing
ATTO 594 DMPE is used to functionalize or probe lipid-coated biomaterials and membrane-mimetic surfaces where fluorescent contrast helps evaluate surface coverage and spatial organization. Materials scientists incorporate the dye-lipid into supported lipid layers, coatings, or lipid-functionalized interfaces to visualize how lipid phases form and remain associated with the substrate. This approach supports microscopy-based assessment of surface uniformity, coating stability, and dynamic changes during incubation or exposure to biomolecular components.
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