AmpliSeq for Illumina Library PLUS and Indexes are optimized for use with Illumina sequencers, and generate highly accurate data with an extensive menu of ready-to-use or made to order content.
Take advantage of low input from as little as 1 ng and flexible input ranges from 1 to 100 ng. Start with either high-quality DNA/RNA samples or use formalin-fixed, paraffin-embedded (FFPE) tissues.
Library preparation with AmpliSeq for Illumina is fast and simple. A multiplexed, polymerase chain reaction (PCR)-based workflow replaces nonspecific hybridization steps, resulting in a high-specificity, high-uniformity amplified library. Multiple genes can be analyzed in a single assay, saving time and reducing costs. Increase lab efficiency with an easy workflow at as low as 5 hours library preparation workflow and only 1.5 hours of hands-on time.
This scalable solution has multiple options for sequencing platforms, data analysis, and support to meet virtually all throughput needs.
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