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68321

Sigma-Aldrich

Atto 390 azide

BioReagent, suitable for fluorescence, ≥90% (HPLC)

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About This Item

Formule empirique (notation de Hill):
C28H41N5O6
Poids moléculaire :
543.66
Code UNSPSC :
12352125
ID de substance PubChem :
329760806
Nomenclature NACRES :
NA.32

Gamme de produits

BioReagent

Pureté

≥90% (HPLC)

Forme

solid

Fabricant/nom de marque

ATTO-TEC GmbH

λ

in ethanol (with 0.1% trifluoroacetic acid)

Absorption UV

λ: 380-384 nm Amax

Adéquation

suitable for fluorescence

Température de stockage

−20°C

Chaîne SMILES 

CC(CC(C)(C)N1CCCC(NCCOCCOCCOCCN=[N+]=[N-])=O)C2=C1C=C(OC(C=C3C)=O)C3=C2

InChI

1S/C28H41N5O6/c1-20-16-27(35)39-25-18-24-22(17-23(20)25)21(2)19-28(3,4)33(24)9-5-6-26(34)30-7-10-36-12-14-38-15-13-37-11-8-31-32-29/h16-18,21H,5-15,19H2,1-4H3,(H,30,34)

Clé InChI

FEBSRHTZZIMYNR-UHFFFAOYSA-N

Description générale

Atto 390 is a fluorescent label with a coumarin structure. The dye is intended for application in the area of life science, e.g. labeling of DNA, RNA or proteins. Characteristic features of the label are high fluorescence quantum yield, large Stokes-shift, good photostability and low molecular weight.
The azide modification is suitable for reactions with alkyne groups (Huisgen reaction - “Click Chemistry“).

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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)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Cuifang Kuang et al.
The Review of scientific instruments, 81(5), 053709-053709 (2010-06-03)
Stimulated emission depletion (STED) microscopy is one of the breakthrough technologies that belong to far-field optical microscopy and can achieve nanoscale spatial resolution. We demonstrate a far-field optical nanoscopy based on continuous wave lasers with different wavelengths, i.e., violet and
Qiang Li et al.
The journal of physical chemistry. B, 115(46), 13643-13649 (2011-10-15)
Fluorescence resonance energy transfer (FRET) using biotinylated β-galactosidase (βGAL) as a donor and Alexa Fluor 350 (AF350) labeled avidin as an acceptor has been investigated by means of steady-state fluorescence and time-resolved fluorescence spectroscopy. The donors are readily paired with
Simon Corrie et al.
Molecular bioSystems, 5(3), 262-268 (2009-02-20)
Herein we report a method for the detection of methylated CpG dinucleotides located within CpG islands in genomic DNA using multiplexed bead-based assays and standard flow cytometry instrumentation. Four CpG "clusters" were identified in the TFPI2 and SPARC CpG islands
Philip Howes et al.
Journal of the American Chemical Society, 132(11), 3989-3996 (2010-02-24)
Semiconducting polymer nanospheres (SPNs) have been synthesized and encapsulated in phospholipid micelles by a solvent evaporation technique. Four different conjugated polymers were used, yielding aqueous dispersions of nanoparticles which emit across the visible spectrum. The synthesis was simple and easily
Gerhild Zauner et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 13(25), 7085-7090 (2007-06-20)
A fluorescence-based system to sense oxygen in solution is described. The method exploits the sensitivity of the endogenous fluorescence of type-3 copper proteins towards the presence of oxygen by translating the near-UV emission of the protein to label fluorescence in
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