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75784

Sigma-Aldrich

Atto 565

BioReagent, suitable for fluorescence

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About This Item

Fórmula empírica (notación de Hill):
C31H31ClN2O9
Peso molecular:
611.04
MDL number:
MFCD03456130
UNSPSC Code:
12352108
NACRES:
NA.32

product line

BioReagent

Quality Level

100

assay

≥90.0% (HPLC)

form

powder

manufacturer/tradename

ATTO-TEC GmbH

λ

in ethanol (with 0.1% trifluoroacetic acid)

UV absorption

λ: 562.0-568.0 nm Amax

suitability

suitable for fluorescence

storage temp.

−20°C

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Application

Atto-Farbstoffe wurden entwickelt, um den höchsten Ansprüchen an Sensitivität zu genügen. Eine einmalige Kombination von Vorteilen macht sie zu bevorzugten Werkzeugen für alle Arten von Markierungen . Und einige Eigenschaften bieten besondere Vorzüge in der Einzelmoleküldetektion. Atto-Farbstoffe basieren auf rigiden Strukturen und zeigen keine cis-trans-isomerisierung. Letztere vermindert bei vielen anderen Fluorophoren die Helligkeit des Signals und führt zur Beeinflussbarkeit durch Umweltbedingungen, bspw. zu spektralen Verschiebungen bei der Konjugation.
Atto 565 hat eine molekulare Absorption von 120.000 und einen QY von 92% in Wasser (97% in Ethanol). Die Abklingzeit beträgt 3.4 ns.
Specific and stable fluorescence labeling of histidine-tagged proteins

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

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Sigma-Aldrich

Sigma-Aldrich

06699

Atto 532

Suman Lata et al.
Journal of the American Chemical Society, 128(7), 2365-2372 (2006-02-16)
Labeling of proteins with fluorescent dyes offers powerful means for monitoring protein interactions in vitro and in live cells. Only a few techniques for noncovalent fluorescence labeling with well-defined localization of the attached dye are currently available. Here, we present
Takao Nakata et al.
The Journal of cell biology, 194(2), 245-255 (2011-07-20)
Polarized transport in neurons is fundamental for the formation of neuronal circuitry. A motor domain-containing truncated KIF5 (a kinesin-1) recognizes axonal microtubules, which are enriched in EB1 binding sites, and selectively accumulates at the tips of axons. However, it remains
Łukasz Krzemiński et al.
Journal of the American Chemical Society, 133(38), 15085-15093 (2011-08-26)
A combined fluorescence and electrochemical method is described that is used to simultaneously monitor the type-1 copper oxidation state and the nitrite turnover rate of a nitrite reductase (NiR) from Alcaligenes faecalis S-6. The catalytic activity of NiR is measured
Marie-Luise Humpert et al.
Proteomics, 12(12), 1938-1948 (2012-05-25)
PTMs of extracellular domains of membrane proteins can influence antibody binding and give rise to ambivalent results. Best proof of protein expression is the use of complementary methods to provide unequivocal evidence. CXCR7, a member of the atypical chemokine receptor
PALM and STORM. Unlocking live-cell super-resolution.
Henriques, R.; Griffiths, C.; Hesper Rego, E.; Mhlanga, Musa M.
Biopolymers, 95(5), 322-331 (2011)
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