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Merck
CN

910147

Sigma-Aldrich

Fluorescein Azide

≥95%

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别名:
4-((3-Azidopropyl)carbamoyl)-2-(6-hydroxy-3-oxo-3H-xanthen-9-yl)benzoesäure, 6-Carboxyfluorescein Azide, 6-FAM azide, N-(3-azidopropyl)-3′,6′-dihydroxy-3-oxo-3H-spiro[isobenzofuran-1,9′-xanthene]-6-carboxamide
经验公式(希尔记法):
C24H18N4O6
分子量:
458.42
MDL编号:
UNSPSC代码:
12352125
NACRES:
NA.22

检测方案

≥95%

形式

powder

反应适用性

reaction type: click chemistry

储存温度

−20°C

应用

This 488nm absorbing dye is probably the most popular dye in cell biology and represents an alternative to Alexa Fluor 488 and the DyLight 488. Fluorescent dye azides can be used for the fluorescent labeling of terminal alkyne-modified molecules by the Cu(I)-catalyzed azide-alkyne (CuAAC) reaction (click reaction).

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Philipp M E Gramlich et al.
Angewandte Chemie (International ed. in English), 47(44), 8350-8358 (2008-09-25)
The attachment of labels onto DNA is of utmost importance in many areas of biomedical research and is valuable in the construction of DNA-based functional nanomaterials. The copper(I)-catalyzed Huisgen cycloaddition of azides and alkynes (CuAAC) has recently been added to
Click-click-click: single to triple modification of DNA.
Philipp M E Gramlich et al.
Angewandte Chemie (International ed. in English), 47(18), 3442-3444 (2008-04-03)

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