and 4.7 μM, respectively, which align well with those from conventional glycosylase-based assays. ABDD also proved to be robust over a broad pH range of 5.5 to 8.5 and enabled accurate measurement in complex cellular lysates. In summary, the ABDD assay establishes a versatile and efficient platform for the functional and kinetic analysis of CDAs, offering a powerful tool with broad applicability in related research fields.
Xu et al. (Mon,) studied this question.