Abstract
This protocol utilises a PCR-ELISA system. Multiple primers are used to amplify HPV L1 sequences by PCR in a conventional thermocycler. Detection of amplification product is achieved by biotinylated probes in a microtitre plate using an ELISA format [3].
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Tabrizi, S.N. (2010). Human Papillomavirus. In: Schuller, M., Sloots, T., James, G., Halliday, C., Carter, I. (eds) PCR for Clinical Microbiology. Springer, Dordrecht. https://doi.org/10.1007/978-90-481-9039-3_44
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DOI: https://doi.org/10.1007/978-90-481-9039-3_44
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