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Immobilization of curcumin on epoxy-sepharose beads and a pull-down assay Epoxy-activated sepharose beads (E6754 Sigma) were incubated with 20 mM curcumin in coupling buffer (50% dimethylformamide, 0.1 M Na 2 CO 3 , and 10 mM NaOH) at 37 C overnight in the dark, and then with 1 M ethanolamine (pH 11) at 37 C overnight to block the remaining non-specific binding sites

doi: 10.1038/s41531-022-00430-8

The concomitant elevation of enzyme and cofactor in AMW50 led us to hypothesize that transaminase activity could be responsible for the D 5 D 4 -glutamate transition observed in Fig

doi: 10.1073/pnas.1102999108 365 TetteFMKwofieSKWilsonMD