Figure 2. Agarose gel electrophoresis of PCR products from Rhinosporidium seeberi–specific primers (A) and β-actin primers (B). The left lane contains a 100-bp ladder. Samples 1–4, from horses with histologic diagnoses of rhinosporidiosis; sample 5, from the skin of a noninfected horse; sample 6, negative control (water).
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