Correspondingly, the excitation wavelengths used were 340 nm for TRY, 480 nm for KN, 434 nm for NFK, and 415 nm for DT
Note that strong chelators, phosphate-rich buffers and reducing agents in an experimental medium will compete for the copper centre and alter the species actually present
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Up to respectively 70 and 40 M, AQ or DEAQ did not significantly activate any of the tested stress response pathways, which is consistent with the limited onset of cytotoxicity by these compounds ( Figure 2 )