A few weeks ago, getting from "I want a His-tagged truncation of my target" to an orderable gene meant three tools, two hours, and a spreadsheet.
Orbion could give you the construct idea — but you still had to look up the tag sequence, pick linkers, assemble everything, run codon optimization, and sanity-check whether the boundaries made sense structurally.
That workflow was slow, brittle, and frankly not how protein work should feel in 2026.
Bench now takes you from target → construct → synthesis-ready DNA in one session.
Go from target to orderable sequence without leaving the platform
- Assembled protein + codon-optimized DNA for every construct
- Tags, linkers, cleavage sites, and fusions resolved to real sequences
- Boundaries annotated and exportable
Know why a construct was designed the way it was
- Boundary decisions tied to pLDDT, disorder, PTMs, and binding sites
- Not "standard domain boundary from literature," but "truncation at residue 85 where pLDDT drops below 70, preserving the predicted binding site at 25–40"
- You control the risk level: conservative designs that match published approaches, or exploratory ones that push toward non-obvious combinations
Compare constructs before committing to the lab
- Scores for boundaries, PTMs, binding, domains, and host fit
- Side-by-side comparison to narrow candidates fast
- Less brute-force screening, more intentional selection
Know what to expect from your protocol before you start
- Timeline expectations with per-step durations
- QC checkpoints with measurable go/no-go criteria
- Yield expectations when supported
If you're starting a new target — or revisiting one that gave you trouble — run it through the updated Bench. Open your dashboard to try it on your own protein.
