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?

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