产品线
BioReagent
方案
≥90% (HPLC)
≥90% (degree of coupling)
表单
solid
制造商/商品名称
ATTO-TEC GmbH
λ
in ethanol (with 0.1% trifluoroacetic acid)
紫外吸收
λ: 597-603 nm Amax
适用性
suitable for fluorescence
储存温度
−20°C
应用
Atto 594 is a novel fluorescent label belonging to the class of Rhodamine dyes. 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, high fluorescence quantum yield, high thermal and photo-stability, excellent water solubility, and very little triplet formation. After coupling to a substrate Atto 594 carries a net electrical charge of -1.
The iodoacetamide derivative reacts, like the maleimide, with a sulfhydryl group forming a thioether bond. It is predominantly used for tagging cystein residues of proteins.
The iodoacetamide derivative reacts, like the maleimide, with a sulfhydryl group forming a thioether bond. It is predominantly used for tagging cystein residues of proteins.
法律信息
This product is for Research use only. In case of intended commercialization, please contact the IP-holder (ATTO-TEC GmbH, Germany) for licensing.
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Massa J Shoura et al.
Nucleic acids research, 40(15), 7452-7464 (2012-05-17)
The Cre-recombination system has become an important tool for genetic manipulation of higher organisms and a model for site-specific DNA-recombination mechanisms employed by the λ-Int superfamily of recombinases. We report a novel quantitative approach for characterizing the probability of DNA-loop
Semi-Solid o/w Emulsions Based on Sucrose Stearates: Influence of Oil and Surfactant Type on Morphology and Rheological Properties.
Klang, V., et al.
Journal of Dispersion Science and Technology, 34, 322-333 (2013)
Michael R Williams et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 32(27), 9228-9237 (2012-07-06)
The potassium channel Kv1.2 α-subunit is expressed in cerebellar Purkinje cell (PC) dendrites where its pharmacological inhibition increases excitability (Khavandgar et al., 2005). Kv1.2 is also expressed in cerebellar basket cell (BC) axon terminals (Sheng et al., 1994), where its
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