HomeFAQsHow much PNGase A should I use to remove my carbohydrate under native or DTT denaturing conditions?
FAQ: How much PNGase A should I use to remove my carbohydrate under native or DTT denaturing conditions?
When the protein is not denatured with SDS, PNGase A has to work harder to reach the cleavage site of the carbohydrate (because of the secondary and tertiary protein structure). Sometimes additional enzyme and extended incubation times can help but these values are specific to each protein and must be determined empirically.
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