Skip to Content
Merck
All Photos(1)

Key Documents

54368

Sigma-Aldrich

Atto 488 DMPE

suitable for fluorescence

Synonym(s):

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

Sign Into View Organizational & Contract Pricing


About This Item

UNSPSC Code:
12352108
NACRES:
NA.32

Assay

≥80.0% (HPCE)
90% (TLC)

Quality Level

form

solid

manufacturer/tradename

ATTO-TEC GmbH

fluorescence

λex 507 nm; λem 527.0 nm±5.0 nm in ethanol

λ

(chloroform/methanol 8:2)

suitability

suitable for fluorescence

storage temp.

−20°C

General description

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.

find more information here

Legal Information

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Breaking the Diffraction Barrier in Fluorescence Microscopy by Optical Shelving.
Bretschneider, S.; Eggeling, Chr.; Hell, S. W.
Physical Review Letters, 98(21) (2007)
Dual color localization microscopy of cellular nanostructures.
Gunkel, M.; et al.
Biotechnology Journal, 4(6), 927-938 (2009)
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)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service