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AMCA-sulfo-NHS

AMCA-Sulfo-NHS Sulfosuccinimidyl-7-amino-4-methylcoumarin-3-acetic acid MW 431... [Pg.432]

AMCA-sulfo-NHS is an analog of AMCA-NHS which contains a sulfonate group on its NHS ring (Thermo Fisher). The negative charge of this group provides enough polarity to... [Pg.432]

Sulfosuccinimidyl-2-(7-azido-4-methylcoumarin-3-acetamide)ethyl-l,3 -dithiopropionate (SAED) is a photoreactive heterobifunctional crosslinking agent that also contains a fluorescent group (Thermo Fisher). The sulfo-NHS ester end of the reagent reacts with primary amines in proteins and other molecules to form stable amide linkages. The photoreactive end is an AMCA... [Pg.316]

Sulfo-SAMCA, sulfosuccinimidyl-7-azido-4-methylcoumarin-3-acetate, is a heterobifunctional reagent similar in design to SAED (Section 3.9, this chapter) (Thermo Fisher). One end of the crosslinker contains an amine-reactive sulfo-NHS ester, while the other end is an AMCA derivative (Chapter 9, Section 3) that contains a photosensitive phenyl azide group. Unlike... [Pg.319]

Three main forms of amine-reactive AMCA probes are commonly available. One of them is simply the free acid form of AMCA, which can be used to couple to amine-containing molecules using the carbodiimide reaction (Chapter 3, Section 1.1). The other two are active-ester derivatives of AMCA—the water-insoluble NHS ester and the water-soluble sulfo-NHS ester forms—both of which spontaneously react with amines to create stable amide linkages. All of them react under mild conditions with primary amines in proteins and other molecules to form highly fluorescent derivatives. [Pg.431]


See other pages where AMCA-sulfo-NHS is mentioned: [Pg.432]    [Pg.434]    [Pg.353]    [Pg.354]    [Pg.333]    [Pg.334]    [Pg.432]    [Pg.434]    [Pg.353]    [Pg.354]    [Pg.333]    [Pg.334]    [Pg.288]    [Pg.292]    [Pg.268]    [Pg.272]    [Pg.1233]    [Pg.743]    [Pg.321]    [Pg.293]    [Pg.273]   


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4 -sulfo

Sulfo-NHS

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