PTG Assembly Designer

Design polycistronic tRNA-gRNA assemblies for CRISPR multiplex editing

How to Use

  1. Select the number of spacers for your assembly (2–9 spacers)
  2. Choose the appropriate gRNA scaffold type for your plant system
  3. Select the Terminal enzyme - used for first & last module only (FokI is default, and supports 11 others)
  4. Select the Golden Gate enzyme - joins all internal modules (BsaI is default, and supports 11 others)
  5. Enter your 20 bp spacer sequences (only A, T, G, C bases allowed)
  6. Click Generate Assembly to compute primer and module designs
  7. View the full results report, which opens in a new browser tab
Tip: Use the Load Example button to see sample sequences and explore a pre-filled assembly design.
  • Automated primer design for all modules
  • Enzymatic Golden Gate cloning with 12 IIs
  • Supports monocot & dicot plant systems
  • Excel / CSV export ready results

Assembly Configuration