910147
Fluorescein Azide
≥95%
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
方案
≥95%
表单
powder
反应适用性
reaction type: click chemistry
储存温度
−20°C
SMILES字符串
[N+](=[N-])=NCCCNC(=O)c1cc(c(cc1)C(=O)O)C2=C3C(=CC(=O)C=C3)Oc4c2ccc(c4)O
InChI
1S/C24H18N4O6/c25-28-27-9-1-8-26-23(31)13-2-5-16(24(32)33)19(10-13)22-17-6-3-14(29)11-20(17)34-21-12-15(30)4-7-18(21)22/h2-7,10-12,29H,1,8-9H2,(H,26,31)(H,32,33)
InChI key
SJAGNCADRVABJA-UHFFFAOYSA-N
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).
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
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)
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
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