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Assay
≥80% (coupling to thiols)
Quality Level
form
solid
manufacturer/tradename
ATTO-TEC GmbH
fluorescence
λex 619 nm; λem 643 nm in 0.1 M phosphate pH 7.0
suitability
suitable for fluorescence
storage temp.
−20°C
General description
Atto 620 belongs to a new generation of fluorescent labels for the red spectral region. The dye is designed for application in the area of life science, e.g. labelling of DNA, RNA or proteins. Characteristic features of the label are strong absorption, temperature dependent fluorescence, high thermal and photo-stability, good water
solubility, and very little triplet formation. Atto 620 is a cationic dye. After coupling to a substrate the dye carries a net electrical charge of +1. In common with most Atto-labels, absorption and fluorescence are independent of pH, at least in the range of pH 2 to 11, used in typical applications.
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solubility, and very little triplet formation. Atto 620 is a cationic dye. After coupling to a substrate the dye carries a net electrical charge of +1. In common with most Atto-labels, absorption and fluorescence are independent of pH, at least in the range of pH 2 to 11, used in typical applications.
find more information here
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
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
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Maria Strianese et al.
Inorganic chemistry, 51(21), 11220-11222 (2012-10-18)
Fluorescently labeled cobalt peptide deformylase (Co-PDF) can be efficiently used as a fluorescence-resonance-energy-transfer-based sensing device for hydrogen sulfide (H(2)S). The proof of concept of our sensor system is substantiated by spectroscopic, structural, and theoretical results. Monohydrogen sulfide coordination to Co-PDF
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This study presents the use of flow cytometry as a high-throughput quantifiable technique to study multicomponent adsorption interactions between proteins and surfaces. Flow cytometry offers the advantage of high-throughput analysis of multiple parameters on a very small sampling scale. This
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