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文献和实验Fluorimetric and HPLC-Based Dengue Virus Protease Assays Using a FRET Substrate
of new lead structures. In this chapter, we describe two dengue virus protease assays based on an internally quenched, high-affinity F�rster resonance energy transfer (FRET) substrate (K m = 105 μM). A fluorimetric assay using a microtiter fluorescence
Visualization of Kinase Activity with FRET‐Based Activity Biosensors
binding between the phosphorylated substrate and phosphoamino acid‐binding domain (PAABD), results in a change in FRET. View Image
Detection of Receptor Heteromers Involving Dopamine Receptors by the Sequential BRET-FRET Technology
to be identified. In SRET experiments, the oxidation of a Renilla Luciferase substrate triggers acceptor excitation by BRET and subsequent energy transfer to a FRET acceptor. Using this methodology here we describe the heteromerization between adenosine A2
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