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18620

Atto 633

Name: Atto 633
Brand: SIGMA

BioReagent, suitable for fluorescence

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About This Item

UNSPSC Code:

12352116

NACRES:

NA.32

MDL number:

MFCD09265385

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product line

BioReagent

Quality Level

100

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 A_max

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

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

18620-1MG:

jan

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Lot/Batch Number

1368196

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satFRET: estimation of Förster resonance energy transfer by acceptor saturation.

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

Home-built integrated microarray system (IMAS). A three-laser confocal fluorescence scanner coupled with a microarray printer.

Sotirios S Tragoulias et al.

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

Myoglobin as a new fluorescence probe to sense H2S.

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

A quantitative measure for alterations in the actin cytoskeleton investigated with automated high-throughput microscopy.

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.

Phospholipids as an alternative to direct covalent coupling: surface functionalization of nanoporous alumina for protein recognition and purification.

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

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