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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 ±10 |
| Properties Quality Level | 100 |
| Storage | −20 °C |
Application
ATTO 594 DOPE is a fluorescent lipid probe built on the DOPE (dioleoylphosphatidylethanolamine) scaffold, enabling membrane incorporation for studies that require robust red-channel fluorescence. Its ATTO 594 dye provides bright emission for tracking lipid mixing, membrane organization, and surface-accessible membrane dynamics in model membranes and cell-associated systems. The lipid nature of ATTO 594 DOPE makes it especially useful when the experimental readout depends on lateral distribution within bilayers rather than covalent labeling of biomolecules.
1. Membrane Labeling Studies
ATTO 594 DOPE is used to fluorescently label lipid bilayers for imaging workflows that focus on membrane organization, lipid diffusion, and phase behavior in supported lipid bilayers, giant unilamellar vesicles, and other membrane-mimetic platforms. Researchers typically incorporate the probe into lipid mixtures to visualize where the dye partitions within the membrane and how lipid domains evolve under experimental perturbations. This lipid-based labeling approach is particularly valuable when the goal is to monitor membrane-associated processes without introducing protein-specific labeling chemistry.
2. Lipid Mixing And Fusion Assays
ATTO 594 DOPE supports fluorescence-based assays designed to quantify lipid mixing during vesicle fusion and related membrane remodeling events. In these workflows, the probe is incorporated into one or more lipid populations so that changes in fluorescence distribution report on fusion-dependent redistribution and membrane mixing. Common use cases include monitoring kinetics in vesicle fusion experiments and comparing conditions that alter membrane curvature, lipid composition, or fusion propensity using red fluorescence readouts compatible with standard fluorescence microscopes and plate readers.
3. Cell Membrane Imaging
ATTO 594 DOPE is applied as a membrane-incorporating dye for cellular imaging experiments where visualization of the plasma membrane or cell-associated membranes is required. By leveraging the DOPE lipid scaffold, the probe can integrate into lipid environments to enable tracking of membrane-associated structures and dynamics with ATTO 594 emission in the red spectral region. This makes ATTO 594 DOPE a practical reagent for microscopy studies that require lipid-localized fluorescence rather than antibody-based staining or genetically encoded reporters.
4. Vesicle Trafficking Visualization
ATTO 594 DOPE is also used in fluorescence microscopy and flow cytometry sample preparation workflows that aim to follow vesicle-associated membranes and trafficking-related redistribution of labeled lipid content. Researchers incorporate the probe into vesicle membranes or membrane fractions and then image or quantify fluorescence changes as vesicles interact with cellular compartments. The lipid labeling strategy helps maintain a membrane-relevant signal source, supporting experiments where the readout depends on where membrane material goes rather than on labeling a specific protein target.
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