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TAMRA alkyne, 5-isomer,945928-17-6,5-TAMRA alkyne

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更新時(shí)間:2024-01-26 10:51:26瀏覽次數(shù):413次

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CAS 945928-17-6 純度 95%+
分子量 467.52 分子式 C28H25N3O4
供貨周期 現(xiàn)貨 規(guī)格 1克 5克 10克
應(yīng)用領(lǐng)域 生物產(chǎn)業(yè) 主要用途 產(chǎn)品僅用于工業(yè)應(yīng)用或者科學(xué)研究等非醫(yī)療目的,不可用于人類或動(dòng)物的臨床診斷或治療
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TAMRA alkyne, 5-isomer,945928-17-6,5-TAMRA alkyne

中文名稱:5-羧基四甲基羅丹明-炔烴

     5-四甲基羅單明炔基化物

其它名稱5-TAMRA alkyne

     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(jiǎn)介:The red-fluorescent tetramethylrhodamine 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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TAMRA alkyne, 5-isomer,945928-17-6,5-TAMRA alkyne


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