It is a component of the DNA polymerase delta complex.

This was subsequently confirmed by analysis of their DNA polymerases.

However, at the protein sequence level, their DNA polymerases share 42% identity.

Error correction is a property of some, but not all, DNA polymerases.

Unlike most DNA polymerases it does not require a template.

This is done in a lab, using an enzyme called DNA polymerase.

A thermostable DNA polymerase is added to the same tube.

DNA polymerase was first isolated from T. aquaticus in 1976.

DNA polymerase can add free nucleotides only to the 3' end of the template strand.

No known DNA polymerase is able to begin a new chain (de novo).

DNA polymerase's rapid catalysis is due to its processive nature.

In the first step, DNA polymerase encounters the direct repeat during the replication process.

One end of the full length strand is linked to the viral DNA polymerase.

DNA polymerases occasionally incorporate mismatch bases into the extending strand.

Various DNA polymerases are extensively used in molecular biology experiments.

The DNA polymerase can start replication at that point and go to the end of the initiation site.

Mitochondrial DNA polymerase may not recognize it as a substrate.

This part is easy, since DNA polymerases can only add nucleotides to an existing strand.

DNA polymerases and ligases fill in the gap using the normal strand as a template.

This can often happen in microsatellite regions due to the DNA polymerase slipping.

The virus carries DNA polymerase which is used to transcribe its genes.

The hairpin at the 3' end serves as a primer for the DNA polymerase.

The DNA polymerase incorporates nucleotides to fill in any gaps.

Gap filling reaction is achieved with DNA polymerase, using all four nucleotides.

Viral strains resistant to vidarabine show changes in DNA polymerase.