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. 2011 Nov 30;2:141–146. doi: 10.2147/RRTM.S27182

Figure 1.

Figure 1

Polymerase chain reaction amplification of 18S SSU rRNA and cytochrome b genes. (A) Nested polymerase chain reaction amplification of the 18S SSU rRNA gene using the primers rPLU3 and rPLU4 matched to all pathogenic Plasmodium species. Lane 1 is a positive control. Lanes 2–11 are products of amplification of 10 monkey blood samples, and lane 12 is a negative control without DNA. (B) The 18S SSU rRNA and the cytochrome b genes were amplified by nested polymerase chain reaction with specific primers to the sequences of Hepatocystis species. Lanes 1 and 2 were the amplicons of 18S SSU rRNA using the primers CHN18-R and CHN18-F and the cytochrome b genes with the primers CHNb 3 and CHNb 4, respectively.