>jane*

Cloning · experimental

Gibson Assembly

Give the tool a vector and one or more inserts and it finds the terminal homology between them, orders the fragments, and builds the assembled product. Detected homology is painted onto the map, so a junction that is too short to anneal is visible rather than implied.

Real vector + insert (40 bp homology) for the Gibson Assembly tool

01

What it does

  1. 01Terminal homology detection between fragments, with the homology length reported per junction
  2. 02Product assembly with annotations carried across from the parent fragments
  3. 03Homology highlighted directly on the plasmid map
  4. 04Fragments taken from the open project, so a PCR product from another tool can go straight in
  5. 05Circular and linear products
02

What it runs on

Assembly runs on the pydna and DnaCauldron ports in packages/ports, golden-tested byte for byte against those Python libraries. The panel runs on @ports/gibson.

Everything runs client-side. Files are parsed in the browser and projects are saved on this machine, so an unpublished sequence is never uploaded.

03

Questions

How much terminal homology does it need?
The homology length is a parameter rather than a fixed constant, and every detected junction reports its own length so a short junction is visible before you build.
Does the product keep the annotations from the parts?
Yes. Features on the parent fragments are carried onto the assembled product and remain editable there.

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