FRET

Development of a novel FRET immunosensor technique

Analytical Chemistry / Biomedical Engineering / Fluorescence / Nanotechnology / Fluorescence Resonance Energy Transfer / Biosensor / Technique / FRET / Resonant Energy Transfer / Protein Complex Detection / Antibody / Reproducibility of Results / Energy Transfer / Sensitivity and Specificity / Equipment Design / Equipment Failure Analysis / P/BV Ratio / Conformational Change / Antigens / Biosensing Techniques / immunoglobulin G / Biosensor / Technique / FRET / Resonant Energy Transfer / Protein Complex Detection / Antibody / Reproducibility of Results / Energy Transfer / Sensitivity and Specificity / Equipment Design / Equipment Failure Analysis / P/BV Ratio / Conformational Change / Antigens / Biosensing Techniques / immunoglobulin G

C-Npys (S-3-nitro-2-pyridinesulfenyl) and peptide derivatives can inhibit a serine-thiol proteinase activity from Paracoccidioides brasiliensis

Fluorescence Resonance Energy Transfer / FRET / Peptides / Biochemical / Affinity chromatography / Fungal Pathogens / Pyridines / PCM / Cysteine endopeptidases / Serine Protease / Therapeutic Use / Paracoccidioides / Biochemistry and cell biology / Molecular Structure / Cysteine Proteinase Inhibitors / Fungal Pathogens / Pyridines / PCM / Cysteine endopeptidases / Serine Protease / Therapeutic Use / Paracoccidioides / Biochemistry and cell biology / Molecular Structure / Cysteine Proteinase Inhibitors
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