Technology

dam-PCR

Dimer Avoided Multiplex PCR

The adaptome, amplified in a single tube

Sequence all 7 B and T cell chains with dimer-avoided multiplex PCR (dam-PCR). This innovative technology uses a patent-pending approach to remove unwanted side product formation during PCR. Dam-PCR increases the signal of particular targets, allowing for unprecedented multiplexing power and all-inclusive sequencing of the immune adaptome.

Dam-PCR is at the core of our RepSeq+ services.

 

Dam-PCR excels at:

  • Multichain analysis
  • Clonotype frequency measurement
  • Dimer removal
  • Bias reduction
  • Error detection

 

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Highly specific amplification

The key to dam-PCR’s specificity is a stringent clean-up step that occurs after the first and second rounds of binding and extension. All unused, sequence-specific primers are removed during clean-up. The final enrichment phase of the PCR uses primers targeting communal tags that are added in the first two cycles.

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Unbiased amplification

Dam-PCR is compatible with the addition of unique molecular identifiers (UMI), which tag individual mRNA molecules. UMIs help identify PCR and sequencing errors for a more quantitative picture of the immune repertoire. Even without UMIs, dam-PCR is highly quantitative because the reaction is focused on the amplicon of interest.

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Reduce costs, reduce time

Our dam-PCR technology is the most cost-effective and cost-saving technology on the market because of the multi-chain approach. Save time and money with incomparable results when you incorporate dam-PCR into your workflow.

Applications

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Because dam-PCR provides a holistic view of the immune repertoire, dam-PCR can be used in a wide range of clinical and research applications. Amplify your studies in any of the following areas with dam-PCR:

  • Somatic hypermutation status
  • Clonotype tracking
  • Translational and basic research
  • Oncology
  • Infectious disease
  • Autoimmune disorders
  • And more

Check out our eBook for more information on dam-PCR and our tools for immune sequencing: