>jane*

Cloning

Restriction Digest

Choose enzymes and see what they do to the sequence: every recognition site on both strands, the fragments a digest produces, and those fragments as bands on a virtual gel. Circular sequences are cut as circles, so a fragment that spans the origin has the length it would really have.

Phage λ plus five plasmids from 2.2 to 7.3 kb: run the λ/HindIII marker you build from its own sequence, beside real digests at an adjustable agarose percentage

01

What it does

  1. 01Recognition sites from the bundled REBASE dataset, matched with full IUPAC degeneracy
  2. 02Circular-aware cutting, so an origin-spanning fragment gets its true length
  3. 03Fragment table with lengths and ends
  4. 04Multi-lane virtual gel at an adjustable agarose percentage, against real molecular-weight ladders
  5. 05Single-cutter filtering, for choosing an insertion site
  6. 06Fragments opened as their own sequences, or sent to the gel bench
02

What it runs on

Digestion runs on the pydna port; gel migration uses a published log-linear mobility law, golden-validated rather than fitted by eye. The panel runs on @ports/enzymes, @ports/gel, @ports/rebase.

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

Does it handle degenerate recognition sequences?
Yes. Sites are matched with full IUPAC degeneracy, so an enzyme whose site contains N, R, Y or W matches every sequence it really matches.
Can I see the digest as a gel?
Yes. Fragments can be rendered as bands on a multi-lane virtual gel at an adjustable agarose percentage, next to real molecular-weight ladders.

Also searched as

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