| Literature DB >> 8253985 |
E Tamburrini1, P Mencarini, A De Luca, A Antinori, E Visconti, A Ammassari, L Ortona, E Ortona, A Siracusano, G Vicari.
Abstract
Two amplification steps were made to detect Pneumocystis carinii DNA by polymerase chain reaction (PCR). pAZ102-E and pAZ102-H (standard PCR), pAZ102-L2 (sense), and pAZ102-E (antisense) (two-step PCR) were used as primers. The amplification products were analyzed by ethidium bromide. After the two-step PCR, ethidium bromide detected all samples positive by oligohybridization after one amplification step. Our two-step PCR is a rapid, cost-effective, and clinically suitable method for the detection of P. carinii infection.Entities:
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Year: 1993 PMID: 8253985 PMCID: PMC266016 DOI: 10.1128/jcm.31.10.2788-2789.1993
Source DB: PubMed Journal: J Clin Microbiol ISSN: 0095-1137 Impact factor: 5.948