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Fig. 2 | BMC Pulmonary Medicine

Fig. 2

From: Pneumocystis jirovecii colonization and its association with pulmonary diseases: a multicenter study based on a modified loop-mediated isothermal amplification assay

Fig. 2

Comparison of the sensitivity of real-time fluorescence LAMP assay and conventional PCR using 10-fold serial dilutions of recombinant plasmid DNA containing P. jirovecii 18S rRNA gene. a Amplification plots of the real-time fluorescence LAMP assay (from 1 × 1010 copies/μl for curve 1 to for 1 × 100 copies/μl curve 11, and no template control for curve 12). b 2% agarose gel electrophoresis of LAMP products from serial dilutions of plasmid from 1 × 1010 copies/μl for lane 1 to for 1 × 100 copies/μl lane 11. M, DNA size marker. c 2% gel electrophoresis of conversional PCR products from serial dilutions of plasmid from 1 × 1010 copies/μl for lane 1 to for 1 × 100 copies/μl lane 11. M, DNA size marker

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