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Product Introduction
ATTO 532 is a fluorescent label related to the well-known dye Rhodamine 6G. Characteristic features of the label are strong absorption, high fluorescence quantum yield, high photostability, and excellent water solubility. Thus ATTO 532 is highly suitable for single-molecule detection applications and high-resolution microscopy such as PALM, dSTORM, STED etc. Additionally the dye highly qualifies to be applied in flow cytometry (FACS), fluorescence in-situ hybridization (FISH) and many more. The fluorescence is excited most efficiently in the range 515-545 nm.A suitable excitation source for ATTO 532 is the 532 nm output of the frequency-doubled Nd:YAG laser.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-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) |
Product Specification
| Excitation | 537 |
| Emission | 559 ±5 |
| Properties Quality Level | 100 |
| Storage | −20 °C |
Application
ATTO 532 DOPE is a lipophilic ATTO 532 fluorescent dye formulated as a DOPE (1,2-dioleoyl-sn-glycero-3-phosphoethanolamine) conjugate, enabling robust membrane incorporation into lipid bilayers. This dye-lipid construct is widely used to generate stable, bright fluorescence labeling of model membranes and membrane-containing biomaterials for fluorescence imaging and quantitative fluorescence assays. Its emission in the visible range makes it a practical choice for standard confocal and widefield fluorescence workflows where a red/orange-emitting lipid dye is required.
1. Membrane Labeling Studies
ATTO 532 DOPE is frequently used to fluorescently label lipid bilayers in supported lipid bilayers, liposomes, and vesicle systems for studying membrane organization, lipid mixing, and vesicle trafficking in vitro. Researchers incorporate the dye-lipid during vesicle formation or during bilayer assembly to obtain uniform membrane-associated fluorescence that tracks membrane integrity during imaging. Because the probe is anchored through the DOPE lipid, it is commonly selected for experiments where the fluorescence should remain localized to the membrane rather than diffuse into the aqueous phase.
2. Liposome Tracking And FRET
ATTO 532 DOPE is used as a membrane donor fluorophore in FRET-based experiments that monitor proximity-dependent interactions between liposomes, membrane proteins, or lipid domains. In these workflows, ATTO 532 DOPE is co-formulated with an appropriate complementary acceptor dye or quencher-labeled lipid to enable distance-sensitive readouts of membrane mixing or association events. This approach is commonly applied in membrane biophysics and chemical biology studies where ratiometric or sensitized emission strategies are used to quantify interaction dynamics.
3. Biomaterial Surface Imaging
ATTO 532 DOPE is also applied for fluorescence visualization of membrane-mimetic coatings and lipid-functionalized biomaterials, including lipid-coated nanoparticles and polymer-supported membrane layers. Materials scientists and biointerface researchers use the dye-lipid to confirm surface coverage, assess coating uniformity, and follow structural changes under experimental conditions using fluorescence microscopy. The DOPE lipid component supports integration into lipid-containing surfaces, making it a convenient tool for correlating material morphology with fluorescent labeling patterns in imaging-based characterization.
4. Flow Cytometry Lipid Assays
ATTO 532 DOPE is leveraged in flow cytometry workflows that quantify fluorescence associated with membrane-bearing particles, such as liposomes or extracellular vesicle-like vesicles, when membrane labeling is needed for population-level analysis. By staining membrane-containing samples with the dye-lipid, researchers can track relative fluorescence intensity across samples to support assay development and comparative studies of labeling consistency and particle-associated fluorescence. This application is commonly used in analytical biochemistry and materials characterization where membrane-associated fluorescence provides a convenient quantitative signal for gating and comparison.
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