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78493

Sigma-Aldrich

Atto 610

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

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About This Item

Formula empirica (notazione di Hill):
C25H31ClN2O6
Peso molecolare:
490.98
Numero MDL:
Codice UNSPSC:
12352108
ID PubChem:
NACRES:
NA.32

Nome Commerciale

BioReagent

Saggio

≥90% (HPLC)

Stato

powder

Produttore/marchio commerciale

ATTO-TEC GmbH

λ

in ethanol (with 0.1% trifluoroacetic acid)

Assorbanza UV

λ: 614-620 nm Amax

Compatibilità

suitable for fluorescence

Temperatura di conservazione

−20°C

Stringa SMILE

[O-]Cl(=O)(=O)=O.C\[N+](C)=C1/C=CC2=Cc3cc4CCCN(CCCC(O)=O)c4cc3C(C)(C)C2=C1

InChI

1S/C25H30N2O2.ClHO4/c1-25(2)21-15-20(26(3)4)10-9-17(21)13-19-14-18-7-5-11-27(12-6-8-24(28)29)23(18)16-22(19)25;2-1(3,4)5/h9-10,13-16H,5-8,11-12H2,1-4H3;(H,2,3,4,5)
SLQQGEVQWLDVDF-UHFFFAOYSA-N

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Applicazioni

Atto labels are designed for highest sensitivity applications. A unique combination of advantages makes them highly favorable tools for all kinds of labeling applications. And some of their properties make them specifically interesting for single molecule detection. Atto labels are based on rigid structures and do not show any cis-trans-isomerization, which lowers brightness of signals and leads to environment dependency, e.g., spectral shifts by conjugation.
Atto 610 shows an molar extinction of 110,000 and QY of 70% in water (70% in ethanol). Decay time is 3.3 ns.

Note legali

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

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)


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Jessica L Felhofer et al.
Electrophoresis, 31(15), 2469-2486 (2010-07-29)
Over the last years, there has been an explosion in the number of developments and applications of CE and microchip-CE. In part, this growth has been the direct consequence of recent developments in instrumentation associated with CE. This review, which
Xiao X Han et al.
Analytical chemistry, 80(17), 6567-6572 (2008-07-30)
A simple and effective protocol for detections of protein-protein and protein-small molecule interactions has been developed. After interactions between proteins and their corresponding ligands, we employed colloidal silver staining for producing active substrates for surface-enhanced Raman scattering (SERS) and surface-enhanced
Lu Liu et al.
Biochemistry, 45(36), 10865-10872 (2006-09-07)
Serpins regulate serine proteases by forming metastable covalent complexes with their targets. The protease docks with the serpin and cleaves the serpin's reactive center loop (RCL) forming an acylenzyme intermediate. Cleavage triggers insertion of the RCL into beta sheet A
Lu Liu et al.
Protein science : a publication of the Protein Society, 16(11), 2403-2411 (2007-10-27)
Serpins inhibit serine proteases by mechanically disrupting the protease active site. The protease first reacts with the serpin's reactive center loop (RCL) to form an acylenzyme. Then the RCL inserts into a beta-sheet in the body of the serpin, translocating
A membrane-bound antiparallel dimer of rat islet amyloid polypeptide.
Abhinav Nath et al.
Angewandte Chemie (International ed. in English), 50(46), 10859-10862 (2011-09-29)

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