Improved tolerance to PCR inhibitors results in higher success rates and streamlined workflows with common E. coli and S. cerevisiae strains*
Improved resistance to many inhibitors commonly found in crude samples—such as denatured protein, salts and metabolites—results in higher PCR success rates and more streamlined workflows*
Improved resistance to inhibitors co-purified in plant DNA extracts, and amplification directly from plant tissues enable higher-throughput workflows and eliminate the need for expensive and time-consuming purification*
Increased throughput and decreased turnaround time*
Better performance compared to other available crude extraction methods *
Robust performance, shorter cycling times, streamlined workflows and higher success rates across a wide variety of template types and amplicons*
Robust performance, shorter cycling times, streamlined workflows and higher success rates across a wide variety of template types and amplicons*
Reduced PCR cycling times and improved success rates streamline workflows for routine genotyping*
High quality and optimal formulation for routine genotyping applications
Increased throughput and decreased turnaround time*
Better performance compared to other available crude extraction methods*
Robust performance across a wide range of GC- and AT-rich templates streamlines workflows while reducing turnaround times. Recommended for end-point applications using gel electrophoresis
Broad coverage of both AT- and GC-rich targets consolidates protocols and reduces cycling times. Recommended for higher sensitivity detection such as capillary electrophoresis and Sanger sequencing workflows