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. 1998 Oct;64(10):3724–3730. doi: 10.1128/aem.64.10.3724-3730.1998

TABLE 4.

Reproducibility of PCR amplification of a single template in a complex mixture of nucleic acids from a natural communitya

Prepn V. anguillarum/(eu)bacterial 16S rDNA ratiob
10% V. anguillarum 1% V. anguillarum 0.1% V. anguillarum
PCR 1 0.156 ± 0.008 0.017 ± 0.001 NDc
PCR 2 0.147 ± 0.011 0.020 ± 0.000 ND
PCR 3 0.153 ± 0.005 0.016 ± 0.001 ND
a

The data were generated by dot blot hybridization by using the V. anguillarum-specific probe Van219 and the universal (eu)bacterial probe S-D-Bact-0338-a-A-18. PCR products were amplified from nucleic acids extracted from a natural community to which known amounts of V. anguillarum DNA were added. 

b

Means ± standard deviations were calculated from data for three replicate dots for each of the samples which was hybridized with the specific probes and quantified by phosphorimaging. 

c

ND, not detected (below detection limit).