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Sigma-Aldrich

Atto 488 Proteinmarkierungs-Kit

BioReagent, suitable for fluorescence

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About This Item

UNSPSC-Code:
12352200
NACRES:
NA.32

Produktlinie

BioReagent

Qualitätsniveau

100

Hersteller/Markenname

ATTO-TEC GmbH

Fluoreszenz

λex 488 nm; λem 520 nm in 0.1 M phosphate buffer, pH 7.0 (recommended)

Eignung

suitable for fluorescence

Lagertemp.

2-8°C

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Allgemeine Beschreibung

Dieser Kit enthält ausreichende Mengen an Reaktivfarbstoff, Puffern und Proteinaufreinigungssets zur Durchführung von 5 Markierungsreaktionen (je 1 mg Protein) und zur nachfolgenden Aufreinigung des markierten Proteins.

Anwendung

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 Protein Labeling Kit is used to produce Atto 488 labeled proteins via conjugation to primary amine groups.

Rechtliche Hinweise

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

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Andrea Pallares Pallares et al.
Food & function, 9(12), 6544-6554 (2018-11-28)
The presence of cell walls entrapping starch granules in common bean cotyledons, prevailing after thermal processing and mechanical disintegration, has been identified as the main reason for their (s)low in vitro starch digestibility. Nevertheless, it is unknown if the role
Switching modulation for protein labeling with activatable fluorescent probes.
Kalyan K Sadhu et al.
Chembiochem : a European journal of chemical biology, 12(9), 1299-1308 (2011-06-02)
Daniela C Dieterich
Current opinion in neurobiology, 20(5), 623-630 (2010-07-24)
Fluorescent proteins have revolutionized cell biology and, therefore, our understanding of the complex molecular and cellular mechanisms that wire the brain together and enable its plasticity throughout life. The ability to visualize cell biological processes has inspired the development of
Gražvydas Lukinavičius et al.
Current opinion in chemical biology, 15(6), 768-774 (2011-11-15)
Numerous synthetic fluorophores have been developed that can switch their spectroscopic properties upon interaction with other molecules or by irradiation with light. In recent years, protein-labeling techniques have been introduced that permit the specific attachment of such molecules to proteins
Lan-Tao Gou et al.
Cell, 180(6), 1212-1227 (2020-03-15)
The paternal genome undergoes a massive exchange of histone with protamine for compaction into sperm during spermiogenesis. Upon fertilization, this process is potently reversed, which is essential for parental genome reprogramming and subsequent activation; however, it remains poorly understood how this
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