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SGLT2 Inhibitor-Induced Euglycemic Diabetic Ketoacidosis: A Case Report
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PCR amplification involved 1 L DNA (25 ng/L), 1.25 L primer (1 l), and 12.5 L of 2x master mix (1.5 mM MgCl, 4.0 mM dNTPs, 2.0 units/L Taq DNA polymerase) in a 25 L reaction volume
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The antioxidant enzymes glutathioneperoxidase, catalase, and superoxide dismutase (SOD) metabolize oxidative toxic intermediates
