Detection was performed using an Applied Biosystems® 3130 Series Genetic Analyzer with a 3 kV 5 s injection. Full profiles were generated at ±20% magnesium concentrations for extracted DNA and swab lysates. Full profiles were observed DZNeP in vitro with FTA® card punches using 1X and +20% magnesium concentrations and with
PunchSolution™-treated nonFTA samples using 1X and −20% magnesium concentrations (Supplemental Table 4). In reactions with FTA® card punches and decreased magnesium, 99% of alleles were called. The D22S1045 alleles dropped out in one of the six FTA® card punch replicates. In the nonFTA punch reactions with a +20% magnesium concentration, 99% of alleles were called, with one of the six replicates yielding low peak heights compared
to the other replicates which caused the DYS391 allele to drop out. Figure options Download phosphatase inhibitor library full-size image Download high-quality image (86 K) Download as PowerPoint slide Minimal artifacts were observed with increased magnesium concentration. Reactions with swab lysates and nonFTA punches showed no additional artifacts with increased magnesium. Extracted DNA and one of two FTA® card donors produced a low-level artifact in D12S381 at 180 bases in the +20% samples that was not present in the 1X magnesium reactions. FTA® card punches from two donors generated a low-level off-ladder artifact in D18S51 at 185 bases that was observed with increased magnesium (data not shown). To determine the effect of primer concentration changes on the PowerPlex® Fusion System results, extracted DNA and FTA® card punches were evaluated with primer concentrations 25% above and below the recommended
concentration. Samples were detected using an Applied Biosystems® 3130 Series Genetic Analyzer with a 3 kV 5 s injection. Full profiles were generated with both extracted DNA and FTA® card punches at all Carbohydrate primer concentrations tested. Little impact was seen on peak heights with variation in primer concentration, and no discrete artifact peaks developed. However, a 25% increase in primer concentration created more minus A product in reactions with extracted DNA than reactions with the recommended primer concentration. This effect was not as pronounced using FTA® card punches. The PowerPlex® Fusion System was developed for human identification STR analysis of casework and reference samples using extracted DNA and solid support substrates. Following SWGDAM and NDIS validation guidelines, 12 forensic and research laboratories demonstrated strong performance throughout validation testing for the PowerPlex® Fusion System. Minimal cross-reactivity, low-level sensitivity and mixture detection, precise and accurate allele calls, and robust performance with casework samples and in the presence of inhibitors were observed. Strong amplification and minimal artifacts were generated under several suboptimal PCR conditions.