product line
BioReagent
Quality Segment
assay
≥90.0% (HPCE)
manufacturer/tradename
ATTO-TEC GmbH
fluorescence
λex 680 nm; λem 695 nm in 0.1 M phosphate pH 7.0
suitability
suitable for fluorescence
storage temp.
−20°C
InChI
1S/C42H57N7O7S2/c1-4-48-18-10-12-27-20-30-35(22-33(27)48)56-36-23-34-29(21-31(36)45-30)28(26-58(53,54)55)24-42(2,3)49(34)19-11-15-39(51)44-17-9-5-8-16-43-38(50)14-7-6-13-37-40-32(25-57-37)46-41(52)47-40/h20-24,32,37,40H,4-19,25-26H2,1-3H3,(H4-,43,44,46,47,50,51,52,53,54,55)/t32-,37?,40-/m0/s1
InChI key
SMZVEGAKSTTZDO-QYIPWQSGSA-N
Application
Atto 680 belongs to a new generation of fluorescent labels. The dye is designed for application in the area of life science, e.g. labeling of DNA, RNA or proteins. Characteristic features of the label are strong absorption, good fluorescence quantum yield, excellent thermal and photo-stability, and very little triplet formation. Atto 680 is a zwitterionic dye with a net electrical charge of zero. The fluorescence is efficiently quenched by electron donors like guanine, tryptophan, etc. Biotin conjugates can be used in applications like ELISA or immunohistochemistry, in situ hybridization, flow cytometry and others, to identify streptavidin, avidin, or extravidin-conjugates.
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.
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
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Slawomir Gwiazda et al.
Biochimie, 94(7), 1457-1463 (2012-04-03)
The RNA-world-theory is one possible explanation of how life on earth has evolved. In this context it is of high interest to search for molecular systems, capable of self-organization into structures with increasing complexity. We have engineered a simple catalytic
The design of a peptide linker group to enhance the SERS signal intensity of an atto680 dye-nanoparticle system.
Drake, P., et al.
Journal of Raman Spectroscopy, 41, 1248-1253 (2010)
Irene Drude et al.
Biochemical and biophysical research communications, 363(1), 24-29 (2007-09-11)
Over the past two decades, the structure and mechanism of catalytic RNA have been extensively studied; now ribozymes are understood well enough to turn them into useful tools. After we have demonstrated the twin ribozyme mediated insertion of additional nucleotides