WE222724-Primer-Designer-Tool

Streamline your workflow with our primer design tool

From design to synthesis, quality primers are vital to successful results. Use our online Applied Biosystems™ Primer Designer™ Tool to search for the right PCR/Sanger sequencing primer pair from a database of ~650,000 predesigned primer pairs for resequencing the human exome and human mitochondrial genome. Choose from different amplicon lengths to accommodate various research applications and biological sample types.

  • Our primers are free of known SNPs and primer-dimers, highly target-specific and used under universal PCR conditions 
  • Full primer coverage for Ion Torrent™ AmpliSeq™ Exome Panel and Ion Torrent™ AmpliSeq™ Cancer Hotspot Panel v.2 Sanger confirmation workflow
  • Flexible primer configuration to meet your research needs: primers can be ordered unmodified, M13-tailed, HPLC-purified or desalted
  • All the primers have been checked by mass spectrometry and have passed stringent bioinformatics metrics; lab bench validation tests have shown >95% success rate

No time for primer design?

From design to synthesis, quality primers are vital to successful results. Search our tool, to find and order pre-designed primers for PCR and Sanger sequencing. Free of SNPs and primer-dimers, highly target-specific, and used under universal PCR conditions - these primers can be ordered unmodified, M13-tailed, HPLC-purified, or desalted. All are checked by mass spectometry. Have confidence knowing primer pairs are selected to tile across exons for optimal exon coverage with a minimal number of primer pairs.

Save time with the Primer Designer™ Tool by selecting from >300,000 primer pairs targeting the human exome.

Primer Designer Tool – Search for PCR & Sanger Sequencing Primers

(File must be less than 500 kb in size and contain less than 1000 unique line-items.)

Fast & powerful data analysis for your genomics platforms

Learn more about our cloud-based Sanger analysis modules
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Primer Designer™ Tool:

Delivery schedule for pre-designed primer pairs.

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Learn about the Sanger sequencing workflow.

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Access software to align Sanger and NGS sequencing files for result confirmation.

Open VR Toolkit™ software

For Research Use Only. Not for use in diagnostic procedures.