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Description
Jun 2012;13(9):1223-1227
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Results Method Development For unbiased analysis of binding to cysteines in recombinant GSTs, each GST was probed for covalent GSH-cysteine adducts, which could have occurred during GST purification over GSH affinity chromatography
Work in the Hughes laboratory is supported by the US National Institutes of Health
The modifications reduce binding to IGF-binding-proteins (IGFBPs), extending plasma half-life dramatically
Lipid peroxidation dysregulation in ischemic stroke: plasma 4-HNE as a potential biomarker
