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Sigma-Aldrich

Atto 488 DOPE

suitable for fluorescence

Synonyme(s) :

1,2-Dioleoyl-sn-glycero-3-phosphoethanolamine labeled with Atto 488

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About This Item

Code UNSPSC :
12352108
Nomenclature NACRES :
NA.32

Pureté

≥90.0% (HPLC)

Niveau de qualité

Forme

solid

Fabricant/nom de marque

ATTO-TEC GmbH

λ

in methanol

Absorption UV

λ: 505.0-511.0 nm Amax

Adéquation

suitable for fluorescence

Température de stockage

−20°C

Description générale

Atto 488 is a labeling dye with high molecular absorption (90,000) and quantum yield (0.80) as well as sufficient Stokes shift between excitation and emission maximum. It is optimized for excitation with an argon laser, and is characterized by high photostability.

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-snglycero-3-phospho-ethanolamine (DMPE) labeled with Atto-dyes.

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Informations légales

This product is for Research use only. In case of intended commercialization, please contact the IP-holder (ATTO-TEC GmbH, Germany) for licensing.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Breaking the Diffraction Barrier in Fluorescence Microscopy by Optical Shelving.
Bretschneider, S.; Eggeling, Chr.; Hell, S. W.
Physical Review Letters, 98(21) (2007)
Super-Resolution Imaging of Fluorophore-Labeled DNA Bound to Gold Nanoparticles. A Single-Molecule, Single-Particle Approach.
Blythe, Karole L.; Willets, Katherine A.
The Journal of Physical Chemistry C, 120(2), 803?815-803?815 (2016)
Effects of Tuning Fluorophore Density, Identity, and Spacing on Reconstructed Images in Super-Resolution Imaging of Fluorophore-Labeled Gold Nanorods.
Blythe, Karole L.; Titus, Eric J.; Willets, Katherine A
The Journal of Physical Chemistry, 119(50), 28099?28110-28099?28110 (2015)
Dynamic Superresolution Imaging of Endogenous Proteins on Living Cells at Ultra-High Density.
Giannone, G.; et al.
Biophysical Journal, 99(4), 1303-1310 (2010)
Instant Live-Cell Super-Resolution Imaging of Cellular Structures by Nanoinjection of Fluorescent Probes.
Hennig, S.; et al.
Nano Letters, 15(2), 1374-1381 (2015)

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