The 3D optical profilometer measurements revealed that the typical height of the microwells were in the range 8–16 µm and opening diameter is in the range 4–8 µm as shown in Fig. 2a. Figure 2b shows an optical micrograph of microwells on PDMS surface with the corresponding individual microwells … See more As explained in Sect. 2, the fluorescence signal from the microwells was recorded and analyzed using fluorescence microscopy. The fluorescence images were acquired from … See more Molecular docking was employed to understand the active sites and forces responsible for interaction between drug and protein. … See more FT-IR spectra of protein exhibited the various amide bonds due to the different vibrations of peptide. Among all amide bonds, amide I is more sensitive to interaction than … See more WebQuenching and dequenching upon interaction with a specific molecular biological target is the basis for activatable optical contrast agents for molecular imaging. [8] [9] Many dyes …
How can I study interaction of BSA (Bovine Serum albumin) with …
WebJul 22, 2024 · One is the dynamic quenching process caused by the random encounter between the excited fluorophore and the quenching agent (ligand) molecules. The other is a static quenching process in which a non-fluorescent ground state complex is formed between the protein and the quenching agent [19,20]. The results of fluorescence … WebJul 8, 2024 · Naik, P. N., Chimatadar, S. A. & Nandibewoor, S. T. Interaction between a potent corticosteroid drug-dexamethasone with bovine serum albumin and human serum … f2hfd1
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WebThe fluorescence of BSA was more effectively quenched by negative CdS nanoparticles than by positive or neutral CdS ones. The quenching degree increased linearly with … WebJan 17, 2024 · Fluorescence quenching is a physicochemical process that lowers the intensity of emitted light from fluorescent molecules. When a molecule absorbs light, electrons in its constituent atoms become ... WebOct 29, 2010 · The interactions of the phenolic acids cinnamic acid (CNA), ferulic acid (FA), caffeic acid (CA) and chlorogenic acid (CLA) with bovine serum albumin (BSA) were investigated and compared using affinity capillary electrophoresis (ACE) and the fluorescence quenching methods. ACE gives binding constants (K b) and … f 2h -f h /h