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Merck
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文件

910147

Sigma-Aldrich

Fluorescein Azide

≥95%

同義詞:

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

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About This Item

經驗公式（希爾表示法）:
C24H18N4O6
CAS號碼:
1386385-76-7
分子量：:
458.42
MDL號碼:
MFCD18426596
分類程式碼代碼:
12352125
NACRES:
NA.22

化驗

≥95%

形狀

powder

反應適用性

reaction type: click chemistry

儲存溫度

−20°C

相關類別

應用

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).

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

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分析證明 (COA)

Lot/Batch Number
MKCN9304
MKCM7954
MKCM3649

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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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