5-羧基四甲基羅丹明 炔烴（945928-17-6） 是炔烴反應(yīng)熒光試劑，用于標(biāo)記包含疊氮化物的生物分子通過非常較有名的鏈接化學(xué)反應(yīng)（炔基與疊氮反應(yīng)）。它與其它TRITC標(biāo)記的生物軛合物具有相同的光譜性能,因此所有可以應(yīng)用TRITC標(biāo)記的設(shè)定同樣適用于5-TAMRA 炔烴標(biāo)記的偶聯(lián)物。

5-羧基四甲基羅丹明 炔烴(945928-17-6)

 

英文名稱：5-TAMRA alkyne

中文名稱：5-羧基四甲基羅丹明-炔烴

其它名稱：5-Carboxytetramethylrhodamine-Alkyne

CAS NO：945928-17-6

分子式：C28H25N3O4

分子量：467.52 g/mol

溶解性：Soluble in DMSO

含 量：95%+

外 觀：固體粉末

保存方法：-20避光避濕

Ex/Em:555/575

結(jié)構(gòu)式：

 

產(chǎn)品簡介:The red-fluorescent tetramethylrhodamine (TAMRA) alkyne can be reacted with azides via a copper-catalyzed click reaction. Click chemistry describes a class of chemical reactions that use bio-orthogonal or biologically unique moities to label and detect a molecule of interest using a two-step procedure. The two-step reaction procedure involves a copper-catalyzed triazole formation of an azide and an alkyne. Click reactions have several characteristics: the reaction between the detection moieties is efficient; no extreme temperatures or solvents are required; the reaction product is stable; the components of the reaction are bioinert; and perhaps most importantly, no side reactions occur – the label and detection tags react selectively and specifically with one another. Unlike traditional chemical reactions utilizing succinimidyl esters or maleimides that target amines and sulfhydryls – functional groups that are not unique – click chemistry-labeled molecules can be applied to complex biological samples and be detected with unprecedented sensitivity due to extremely low background.

 

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5-羧基四甲基羅丹明 炔烴(945928-17-6)