I had performed catalase assay using Aebi 1984 method, afterwards taking absorption at 240 nm for 1 minute. I put my OD in formula for calculating catalase activity:
ΔA/min x volume of assay mixture (3 ml) x dilution factor x 1000/Volume of sample (ml) x 0.0439 x protein concentration (mg/ml).
But the activity of catalase results in value more than 12,000 and more. Is it correct way to calculate?