Six layers underneath. One workspace on top.

Language models, a kit of real tools, your lab's records and memory, and approval steps work together, so what you use is one connected workspace.

01 · Where the time goes

Same mistake. Caught on Day 0 instead of Day 3.

A Gibson overlap that's too short. Today it can show up as an empty plate and a reorder. In Plasmole, the overlap check flags it while you design.

Example · GFP into pET-28a by Gibson
Todayseparate tools
Designprimers and overlaps worked out across separate tools
Primers ship1–3 working days1
PCR, Gibson, transformplates overnight2
Empty plate12 bp overlap; redesign and reorder
Primers ship again1–3 working days1
PCR, Gibson, transformplates overnight2
Pick, culture12–18 h2
Miniprep, Sangernext business day3
VerifiedDay 8
In Plasmoleone request
Design, checked12 bp overlap flagged; redesigned with 25 bp Gibson primersTmoverlap checkassemblydigestpast entries
Primers ship1–3 working days1
PCR, Gibson, transformplates overnight2
Pick, culture12–18 h2
Miniprep, Sangernext business day3
Verifiedreads checked against the design
3 days backno redo loop
3+ dayssooner to a verified plasmid, if the redo is avoidedAn example with next-day primers; slower delivery widens the gap. Added up from the cited times [1]–[3]; an illustration, not a measured average.
15%of 2,521 lab-made plasmids from labs worldwide had design errors, in a 2025 studyBai et al., Nucleic Acids Research 20254
Handled for youAsk Plasmole to design primers, calculate Tm, check overlaps and assembly, preview a digest and look up past notebook results. The chat shows the tools it calls, with result previews.you approve, order and pipette
  1. Primer turnaround, accessed October 2026: IDT Custom DNA Oligos (over 90% of standard orders ship within 24 hours; next-business-day delivery at the fastest); Eurofins Genomics EU salt-free oligos (1–3 working days); Thermo Fisher desalted primers (within 3 business days).
  2. Addgene protocols, Bacterial transformation (plates overnight at 37 °C) and Inoculating a bacterial culture (12–18 h); Thermo Fisher bacterial transformation workflow.
  3. Sanger turnaround, accessed October 2026: GENEWIZ/Azenta (results by noon the next business day after receipt); Eurofins Genomics (99% of tube results the next morning). Shipping time comes on top.
  4. Bai et al., Nucleic Acids Research 53(14), 2025: of 2,521 lab-made plasmids, 384 (about 15%) had design errors; 91 of 259 sequenced plasmids differed from the sender's reference. Peer reviewed; the authors work for a plasmid vendor.
02 · How it works

Ask about past attempts, then design.

Real turn

Find what your lab tried

Ask in plain words. It searches your notebook.

What did we try for pET-28a Gibsons?
Finished in 3 steps · 25s
  • Searching your labpET-28a Gibson2 results
  • Reading a notebook entryGibson: GFP into pET-28a
  • Reading a notebook entryGibson: sfGFP into pET-28a

Two Gibson attempts are logged, on 14 Aug and 2 Sep. Both gave empty Kan plates while the controls grew, and both used short overlaps: 16 bp, then 18 bp.

Gibson: sfGFP into pET-28aOpen the entry

01 is a real turn in an example lab. 02's check messages and 03's primer numbers are Plasmole's real output; the rest is example data.

04 · What's different

How Plasmole AI is different.

Primer3, Biopython and pydna compute primers, Tm, digests and assemblies. 31 of the 90+ tools are deterministic: the same inputs and settings give the same numbers.

Illustrations with example data

05 · Lab memory

The people rotate. The lab remembers.

Lab Brain keeps what your lab has settled, with the person who taught it attached. Every answer that uses it says so.

Memory ExplorerKim Lab
Search memories…
  • General

    Use Gibson assembly for builds with fewer than 4 parts.

    Taught by Maya Chen · used in 14 conversationsMake privateEditDelete from lab brain
  • General

    Our default strain for cloning is E. coli DH5α.

    Taught by Adi Kulkarni · used in 31 conversationsMake privateEditDelete from lab brain
  • Project

    The mCherry reporter line is on hold until the new stock arrives.

    Taught by Priya Natarajan · used in 3 conversationsMake privateEditDelete from lab brain
Illustration with example data: the lab-wide tier of the Memory Explorer
  • Shared with the lab

    Conventions, defaults and decisions every member's assistant works from. Each one names who taught it.

  • Private to you

    Facts that stay with their author, in that lab. Nobody else's assistant sees them.

  • Follows you

    Your own preferences travel with you between workspaces. Lab memory never leaves its workspace.

  • Yours to review

    Members read everything in the Memory Explorer and edit or delete what they taught it. A lab fact can be made private again.

Questions it answers from memory and records
  • Which strain do we clone in?
  • What did the lab decide about Gibson for small builds?
  • Which projects are on hold, and why?
  • Who ran the last GFP plate, and what was overdue?

Memory is context for lab questions. Designs and sequence analysis run from your records and the tool kit, not from memory.

06 · Questions

What teams ask before they turn it on.

More on how data moves in the security overview.

Can it be wrong?

Yes. It's a language model working with tools. The chat shows the tools it calls with result previews, so check the proposed design before you use it. High-risk actions wait for your approval.

Which models does it use?

The base of our intelligence layer is a frontier model.

Do you train models on our research?

No. Plasmole doesn't train models on your research, and Anthropic and OpenAI state that they don't use API data to train their models by default.

Can it change our data without asking?

High-risk actions, including changes to a sequence, wait on an approval card until you approve them. Some lower-risk actions run directly, such as saving designed primers.

Can we turn it off?

Yes. We switch AI processing off for a workspace when your agreement requires it.