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. 2006 Feb 18;34(4):1102–1111. doi: 10.1093/nar/gkj512

Figure 3.

Figure 3

PCR amplification of the 1.1 kb S.tengchongensis Dpo4-like gene by Dpo4-like polymerases. A total of 2.5 U of Taq or 200 nM (400 nM of Ssh) of each Dpo4-like polymerase was added to the PCRs. Two microliters of the 50 µl PCRs were loaded onto a 0.9% agarose gel and the PCR products separated by electrophoresis. The enzymes employed in the PCRs are specified above each lane. The position of the 1.1 kb PCR product is indicated on the left. L and 100 designates the lambda BstE II and 100 bp markers, respectively.