72998

Sigma-Aldrich

Atto 594 azide

BioReagent, suitable for fluorescence, ≥80.0% (HPCE)

NACRES:
NA.32
Pricing and availability is not currently available.

product line

BioReagent

assay

≥80.0% (HPCE)

fluorescence

λex 601 nm; λem 627 nm±10 nm in 0.1 M phosphate pH 7.0

suitability

suitable for fluorescence

storage temp.

−20°C

Application

Atto 594 is a novel fluorescent label belonging to the class of Rhodamine dyes. The dye is designed for application in the area of life science, e.g. labeling of DNA, RNA or proteins. Characteristic features of the label are strong absorption, high fluorescence quantum yield, high thermal and photo-stability, excellent water solubility, and very little triplet formation. After coupling to a substrate Atto 594 carries a net electrical charge of -1.
The azide modification is used in the Huisgen reaction (“Click Chemistry“).

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.

RIDADR

NONH for all modes of transport

WGK Germany

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificate of Analysis
Certificate of Origin
Semi-Solid o/w Emulsions Based on Sucrose Stearates: Influence of Oil and Surfactant Type on Morphology and Rheological Properties.
Klang, V., et al.
Journal of Dispersion Science and Technology, 34, 322-333 (2013)
Massa J Shoura et al.
Nucleic acids research, 40(15), 7452-7464 (2012-05-17)
The Cre-recombination system has become an important tool for genetic manipulation of higher organisms and a model for site-specific DNA-recombination mechanisms employed by the λ-Int superfamily of recombinases. We report a novel quantitative approach for characterizing the probability of DNA-loop...
Michael R Williams et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 32(27), 9228-9237 (2012-07-06)
The potassium channel Kv1.2 α-subunit is expressed in cerebellar Purkinje cell (PC) dendrites where its pharmacological inhibition increases excitability (Khavandgar et al., 2005). Kv1.2 is also expressed in cerebellar basket cell (BC) axon terminals (Sheng et al., 1994), where its...

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