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Effect of knockout of glutathione peroxidase-1 (GPX1) and... | Download Scientific Diagram
The assay buffer was KME (120 mM KCl, 20 mM MOPS, 1 mM EGTA, pH 7.20) plus 0.02% Triton X-100 and 5 µM rotenone (when the assay was coupled to the production or consumption of NADH)
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To our best knowledge, the study is the first indication of the multiple impacts of Cu(II) on biochemical cycle(s) and pathways that participate in (epi)genetic regulation of GPRE due to in vitro anther tissue cultures
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