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Product Introduction
ATTO 633 belongs to a new generation of fluorescent labels for the red spectral region. The dye is designed for application in the area of life science, e.g. labelling of DNA, RNA or proteins. Characteristic features of the label are strong absorption, high fluorescence quantum yield, high photostability, good water solubility, and very little triplet formation. ATTO 633 is a cationic dye. After coupling to a substrate the dye carries a net electrical charge of +1. In common with most ATTO-labels, absorption and fluorescence are independent of pH, at least in the range of pH 2 to 11, used in typical applications.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 | 629 |
| Emission | 665 ±5 |
| Properties Quality Level | 100 |
| Storage | −20 °C |
Application
ATTO 633 DMPE is a far-red ATTO 633-based fluorescent dye formulated for membrane-associated labeling workflows, leveraging the DMPE lipid motif to support incorporation into lipid environments. Its red-shifted emission is commonly used when researchers need bright, spectrally separated fluorescence for cellular imaging and fluorescence-based assays. In practice, ATTO 633 DMPE is handled as a fluorescent labeling reagent for preparing stained membranes, lipid-containing materials, and dye-loaded probe constructs compatible with standard fluorescence microscopy and plate-reader formats.
1. Membrane Labeling Studies
ATTO 633 DMPE is widely used to label cellular membranes and model lipid systems for imaging and quantitative fluorescence readouts. Researchers incorporate the dye into lipid bilayers to visualize membrane distribution, trafficking-related changes in membrane organization, and dye partitioning behavior in liposomes or supported lipid layers. Because the emission sits in the far-red region, ATTO 633 DMPE is often selected to reduce spectral overlap with common green fluorophores when performing multicolor membrane experiments.
2. Liposome And Nanoparticle Tracing
ATTO 633 DMPE supports fluorescent tracking of lipid nanoparticles, liposomes, and other lipid-containing carriers used in chemical biology and biomaterials research. Teams use dye-loaded vesicles to follow particle association with cells, monitor uptake-related fluorescence changes, and compare relative labeling stability across formulation conditions. The DMPE lipid character helps maintain the dye within lipid assemblies, enabling consistent fluorescence signals for time-course microscopy and plate-based measurements.
3. Fluorescence Microscopy Imaging
ATTO 633 DMPE is frequently chosen for far-red fluorescence microscopy to visualize labeled membranes and lipid components with reduced background from autofluorescence. Imaging groups use the dye for confocal and widefield studies where robust far-red emission improves contrast, particularly in complex biological samples. When combined with other spectrally distinct dyes, ATTO 633 DMPE helps researchers construct multichannel imaging panels for membrane-associated localization and colocalization analyses.
4. Flow Cytometry Lipid Probing
ATTO 633 DMPE is applied in flow cytometry workflows that assess membrane-associated fluorescence intensity in labeled cell populations. Investigators stain cells with lipid-incorporating dye to quantify changes in membrane labeling patterns and to compare relative fluorescence across experimental conditions in a high-throughput format. The far-red spectral window supports multiplexing strategies where green and orange channels are already in use, enabling clearer separation of membrane labeling signals from other fluorophores in the same assay panel.
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