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查看更多产品信息 DyNAzyme II DNA Polymerase (2 U/µL) - FAQs (F501S)
3 个常见问题解答
10% DMSO will inhibit DyNAzyme DNA Polymerases to some extent. This inhibition may be overcome by using twice the amount of DyNAzyme DNA Polymerase.
DyNAzyme II DNA Polymerase can use dUTP, biotinylated dNTPs, 7-deaza-dGTP, digoxigenin-dUTP, bromo-dUTP, radiolabeled dNTPs and ITP. DyNAzyme EXT DNA Polymerase and Phusion DNA Polymerase cannot read dUTP-derivatives or dITP in the template strand so the use of these analogues is not recommended. Use Phusion U Hot Start DNA Polymerase for amplification of dUTP and dITP containing templates.
DyNAzyme DNA Polymerases are capable of adding a 3'-overhang. However, the efficiency at which the extra base is added is sequence-dependent. The extra base is usually A, however, the enzyme can also incorporate other bases or even more than a single base at a sequence-specific manner. To enhance TA-cloning it may be helpful to include an additional incubation period of 10-30 minutes at 72 degrees C to the end of cycle protocol.