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68652

Atto 633 iodoacetamide

suitable for fluorescence

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A propos de cet article

NACRES:
NA.32
UNSPSC Code:
12352200


form

powder

manufacturer/tradename

ATTO-TEC GmbH

fluorescence

λex 629 nm; λem 655 nm in 0.1 M phosphate pH 7.0

suitability

corresponds for coupling to thiols, suitable for fluorescence

storage temp.

−20°C

General description

Atto 633 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, high fluorescence quantum yield, high photostability, good water solubility, and very little triplet formation. Atto 633 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.
The iodoacetamide derivative reacts, like the maleimide, with a sulfhydryl group forming a thioether bond. It is predominantly used for tagging cystein residues of proteins.

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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.


Classe de stockage

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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Thomas D Lazzara et al.
Journal of colloid and interface science, 366(1), 57-63 (2011-10-29)
Anodic aluminum oxide (AAO) substrates with aligned, cylindrical, non-intersecting pores with diameters of 75 nm and depths of 3.5 or 10 μm were functionalized with lipid monolayers harboring different receptor lipids. AAO was first functionalized with dodecyl-trichlorosilane, followed by fusion
Ronny Schmidt et al.
Journal of proteome research, 10(3), 1316-1322 (2011-01-21)
Based on a single-molecule sensitive fluorescence-linked immunosorbent assay, an analytical platform for the detection of lipoarabinomannan (LAM), a lipopolysaccharide marker of tuberculosis, was established that is about 3 orders of magnitude more sensitive than comparable current ELISA assays. No amplification



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