DNA extraction was performed using the ammonium acetate method. One microliter of DNA was used as the template for each polymerase. Most prominently, the strands are synthesized by DNA polymerase by adding.

DNA polymerase I during the sequencing reaction instead of Taq polymerase. DNA replication occurs throughout the S stage of interphase. The DNA polymerase I would denature because the of . USER Enzyme is a mixture of Uracil DNA glycosylase (UDG) and the DNA.

C 11Page of KOD Hot Start DNA Polymerase KOD Hot Start DNA . TaKaRa Taq DNA polymerase (TaKaRa Bio Inc., Tokyo, Japan) was used for all PCR reactions. A negative control without DNA and a positive . Diastereoselective Formal Total Synthesis of the DNA Polymerase α Inhibitor, Aphidicolin, Using Palladium-Catalyzed Cycloalkenylation and Intramolecular . For both (f) and (g) ChIP using antibody against RNA Polymerase II (Pol II) and IgG served as positive and negative control, respectively. Correction: In Silico Screening for Novel Inhibitors of DNA Polymerase III Alpha Subunit of Mycobacterium tuberculosis (MtbDnaE H37Rv).