Rapid Amplification of Plasmid and Phage DNA Using Phi29 DNA Polymerase and Multiply-Primed Rolling Circle Amplification

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Figure 4.
Figure 4.

Effect of exonuclease-resistant random primers on amplification. Annealing reactions (20 μL) were performed as described except that the template DNA was M13 double-strand RF DNA and the primers were either exo-resistant or exo-sensitive hexamers. Reactions contained 1 ng of M13 DNA with exo-resistant or exo-sensitive primers and φ29 DNA polymerase as indicated. Reactions were incubated at 34°C for 13 h. DNA synthesis was quantitated by the incorporation of radioactive nucleotide.

This Article

  1. Genome Res. 11: 1095-1099

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