Abstract
N-(4-(7-diethylamino-4-methylcoumarin-3-yl)phenyl)maleimide (CPM) and the corresponding iodoacetamide are described. When applied to sections at pH 6 and 9, respectively, the two fluorogens are very similar in their reactivity and selectivity toward thiols with which they form adducts having much the same bright blue fluorescence. However, differences in other properties favor CPM for further study.
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CITATION STYLE
Sippel, T. O. (1981). New fluorochromes for thiols: Maleimide and iodoacetamide derivatives of a 3-phenylcoumarin fluorophore. Journal of Histochemistry and Cytochemistry, 29(2), 314–316. https://doi.org/10.1177/29.2.7019305
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