50712
Atto 465
BioReagent, suitable for fluorescence
InChI key
WNDQPKGVFUAMOZ-UHFFFAOYSA-N
SMILES string
OCl(=O)(=O)=O.Nc1ccc2C=C3C=CC(=N)C=C3N(CCCC(O)=O)c2c1
InChI
1S/C17H17N3O2.ClHO4/c18-13-5-3-11-8-12-4-6-14(19)10-16(12)20(15(11)9-13)7-1-2-17(21)22;2-1(3,4)5/h3-6,8-10,18H,1-2,7,19H2,(H,21,22);(H,2,3,4,5)
product line
BioReagent
fluorescence
λex 453 nm; λem 508 nm
suitability
in accordance for fluorescence, suitable for fluorescence
storage temp.
−20°C
General description
Atto 465 is a new label with strong absorption and fluorescence and a large stoke′s shift (excitation maximum 453 nm, emission maximum 508 nm). The dye is characterized by high photostability and thermal stability. The dye is moderately hydrophilic, the NHS-ester and maleimide derivatives are very well soluble in polar solvents as DMSO, DMF or acetonitrile. At low temperatures or embedded into polymeric matrices it shows intense phosphorescence.
Application
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 465 is suitable for preparation of fluorescence labeling reagents and studies of the physicochemical properties of the dye.
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 Information
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Jutta Arden-Jacob et al.
Physical chemistry chemical physics : PCCP, 15(6), 1844-1853 (2012-12-19)
The excited state dynamics of the dye ATTO 465, a well-known fluorescence marker for biological applications, have been characterized in various solvents including THF, ethanol, methanol, water and the highly polar protic ionic liquid 2-hydroxyethylammonium formate (2-OH-EAF) by combining results
Radek Macháň et al.
Analytical and bioanalytical chemistry, 399(10), 3547-3554 (2011-02-05)
Z-scan fluorescence correlation spectroscopy (FCS) is employed to characterize the interaction between arenicin-1 and supported lipid bilayers (SLBs) of different compositions. Lipid analogue C8-BODIPY 500/510C5-HPC and ATTO 465 labelled arenicin-1 are used to detect changes in lipid and peptide diffusion
David J Posson et al.
Nature, 436(7052), 848-851 (2005-08-12)
Voltage-gated ion channels open and close in response to voltage changes across electrically excitable cell membranes. Voltage-gated potassium (Kv) channels are homotetramers with each subunit constructed from six transmembrane segments, S1-S6 (ref. 2). The voltage-sensing domain (segments S1-S4) contains charged
Gerald Donnert et al.
Proceedings of the National Academy of Sciences of the United States of America, 103(31), 11440-11445 (2006-07-26)
We demonstrate far-field fluorescence microscopy with a focal-plane resolution of 15-20 nm in biological samples. The 10- to 12-fold multilateral increase in resolution below the diffraction barrier has been enabled by the elimination of molecular triplet state excitation as a
Waldemar Waldeck et al.
International journal of medical sciences, 8(2), 97-105 (2011-02-01)
Fluorescent proteins (FPs) are established tools for new applications, not-restricted to the cell biological research. They could also be ideal in surgery enhancing the precision to differentiate between the target tissue and the surrounding healthy tissue. FPs like the KillerRed
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