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Metallopeptidase gene expression in extracellular toxoplasmic tachyzoites by RT-PCR.

Products of the expected size were observed for all primers, using either cDNA and gDNA as templates. As a further control for the presence of contaminating gDNA, primers of each gene were designed to amplify fragments of distinct length from cDNA(c) and gDNA(g) due to the presence of introns. Molecular size standards are indicated to the left.

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