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3.7 Quenching of intrinsic fluorescence of BSA by CIPp-18 The 295 nm excited fluorescence spectrum of BSA display peak at ~ 340 nm and is mainly contributed by the two tryptophan residues i.e., Trp134 and Trp213 which are located in the main drug-binding site (Sudlow site I) and the heme-binding site, respectively [51]

Model of the regulation of GPx1 in breast cells by selenium and estrogens