All you need to do to resolve this problem is to dilute some of the extract with an equal volume of the extraction buffer and re-run the assay. In the calculations, simply multiply the activity value by the extra dilution (i.e. X 2 if 2-fold).
In the Limit-Dextrizyme Tablet assay the absorbance value is higher than 1.6. The standard curve in the product datasheet only reaches 1.6. therefore I cannot convert this to milli-units/assay.
Modified on: Thu, 10 May, 2018 at 11:59 AM
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