TABLE 1.
Comparison of standard curves obtained using either water alone or water plus murine DNAa
| Dilution medium and target | Mean Ct at the indicated target copy no.b:
|
ΔRn from plateauc | Sloped | PCR efficiencye (%) | |||||
|---|---|---|---|---|---|---|---|---|---|
| 106 | 105 | 104 | 103 | 102 | 101 | ||||
| Water alone | |||||||||
| HIV-1 | 17.4 | 21.1 | 24.4 | 28.3 | 31.8 | 35.2 | 1.3 | −3.57 | 90 |
| Albumin | 17.4 | 21.6 | 25.0 | 28.7 | 32.3 | 35.7 | 1.9 | −3.60 | 89 |
| Water + murine DNA | |||||||||
| HIV-1 | 18.4 | 21.9 | 25.9 | 29.2 | 32.8 | 35.6 | 1.1 | −3.51 | 92 |
| Albumin | 18.3 | 22.0 | 26.0 | 29.7 | 33.5 | 36.8 | 1.8 | −3.73 | 85 |
The amplification parameters for HIV-1 and albumin quantification were obtained with dilutions ranging from 106 to 101 copies of the double plasmid standard, and experiments were carried out in either water alone or water containing 1 μg of murine DNA from the BALB/3T3 cell line.
Average Ct values measured in duplicate for each point of the calibration curve.
Average values of normalized fluorescence intensity (ΔRn) taken from the plateau of all the amplification curves.
Slopes of the calibration curves.
Percent amplification efficiency, calculated as (10(−1/slope) − 1) × 100.