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Reconstituted solutions should be protected from reducing agents (such as DTT or beta-mercaptoethanol), which can cleave the disulfide bond and disrupt the active conformation

Levet S, Medina J, Joanou J, et al

JS-K and many other NO prodrugs represent an innovative biological approach in the development of anticancer therapeutics

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However, comparison of the H-site residues of GSTs displaying high activity with those having low activity does not identify a signature set of residues conferring the high rates of ketosteroid isomerization (Table 1)

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