I am designing a system in which I am supposed to have a Fluorescein-TAMRA FRET pair on a DNA strand, but on its current configuration I only get non-radiative FRET quenching rather than (the fluorophores are in a DNA duplex and they are both on the same extreme of the duplex, being the distance the closest that the duplex formation allows).  I need to know the Forster radius of the pair in order to know how far can I put one from the other to have the radiative FRET without compromising eficiency too much.

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