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Sigma-Aldrich

Atto 633

BioReagent, suitable for fluorescence

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About This Item

MDL number:
MFCD09265385
UNSPSC Code:
12352116
NACRES:
NA.32

product line

BioReagent

assay

≥90.0% (HPLC)

form

solid

manufacturer/tradename

ATTO-TEC GmbH

λ

in ethanol (with 0,1% trifluoroacetic acid)

UV absorption

λ: 627-633 nm Amax

suitability

suitable for fluorescence

storage temp.

−20°C

Application

Atto 633 is a red-emitting fluorescence label with strong absorption, high quantum yield (64%), high photostability, good water solubility, and very little triplet formation. This label is optimized for use with diode laser excitation at 633 nm and characterized by high photostability.

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)

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Analytical and bioanalytical chemistry, 390(6), 1563-1573 (2008-01-30)
Microarray technology covers the urgent need to exploit the accumulated genetic information from large-scale sequencing projects and facilitate investigations on a genome-wide scale. Although most applications focus on DNA microarrays, the technology has expanded to microarrays of proteins, peptides, carbohydrates
Martin Beutler et al.
European biophysics journal : EBJ, 38(1), 69-82 (2008-09-05)
We demonstrate theoretically and experimentally the quantification of Förster resonance energy transfer (FRET) by direct and systematic saturation of the excited state of acceptor molecules. This version of acceptor depletion methods for FRET estimation, denoted as "satFRET" is reversible and
Maria Strianese et al.
Protein and peptide letters, 18(3), 282-286 (2010-09-23)
A new, fast, simple and cost-effective sensing device for monitoring H(2)S has been developed. Proof-of-principle results showing that a commercial and cheap Myoglobin (Mb) can be successfully used as a biological probe for a fluorescence biosensor for H(2)S detection are
Julian Weichsel et al.
Cytometry. Part A : the journal of the International Society for Analytical Cytology, 77(1), 52-63 (2009-11-10)
The actin cytoskeleton modulates a large variety of physiological and disease-related processes in the cell. For example, actin has been shown to be a crucial host factor for successful infection by HIV-1, but the underlying mechanistic details are still unknown.
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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