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41051

Sigma-Aldrich

Atto 488

BioReagent, suitable for fluorescence, ≥90% (HPLC)

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About This Item

Codice UNSPSC:
12352108
NACRES:
NA.32

Nome Commerciale

BioReagent

Saggio

≥90% (HPLC)

Produttore/marchio commerciale

ATTO-TEC GmbH

λ

in methanol: water (1:1) (with 0.1% perchloric acid)

Assorbanza UV

λ: 501-507 nm Amax

Compatibilità

suitable for fluorescence

Temperatura di conservazione

−20°C

Categorie correlate

Descrizione generale

Atto 488 is a labeling dye with high molecular absorption (90,000) and quantum yield (0.80) as well as sufficient Stokes shift between excitation and emission maximum. It is optimized for excitation with an argon laser, and is characterized by high photostability.

Applicazioni

Atto fluorescent labels are designed for high sensitivity applications, including single molecule detection. Atto labels have rigid structures that do not show any cis-trans-isomerization. Thus these labels display exceptional intensity with minimal spectral shift on conjugation. Atto 488 is suitable for preparation of fluorescence labeling reagents and the study of its physicochemical properties.

Note legali

This product is for Research use only. In case of intended commercialization, please contact the IP-holder (ATTO-TEC GmbH, Germany) for licensing.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Silviya Zustiak et al.
Journal of biomedical optics, 17(12), 125004-125004 (2012-12-05)
Fluorescence correlation spectroscopy (FCS) is increasingly being used to assess the movement of particles diffusing in complex, optically dense surroundings, in which case measurement conditions may complicate data interpretation. It is considered how a single-photon FCS measurement can be affected
Analysis of fluorescent nanostructures in biological systems by means of spectral position determination microscopy (SPDM).
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Current Microscopy Contributions to Advances in Science and Technology, 1, 3-12 (2012)
Monitoring single membrane protein dynamics in a liposome manipulated in solution by the ABELtrap.
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arXiv, 1102-1102 (2011)
Ying Shen et al.
Nature communications, 10(1), 433-433 (2019-01-27)
Aberrant sperm flagella impair sperm motility and cause male infertility, yet the genes which have been identified in multiple morphological abnormalities of the flagella (MMAF) can only explain the pathogenic mechanisms of MMAF in a small number of cases. Here
Mohd A Mohd Ridzuan et al.
PloS one, 7(3), e33845-e33845 (2012-04-06)
An actomyosin motor complex assembled below the parasite's plasma membrane drives erythrocyte invasion by Plasmodium falciparum merozoites. The complex is comprised of several proteins including myosin (MyoA), myosin tail domain interacting protein (MTIP) and glideosome associated proteins (GAP) 45 and
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