RIFT resolves how a compound actually affects transcription — burst by burst, molecule by molecule — so cross-reactivity risk is built to surface on our bench, not in your trial.
Across Phase 1–3, transcription factor and chromatin-targeted candidates fail at some of the highest rates in drug development — not for lack of efficacy, but because off-target and cross-reactivity effects go undetected until they surface in patients. Bulk biochemical assays average across millions of molecules and simply can't see it. By the time a compound reaches the clinic, that blind spot has already cost years and tens of millions of dollars.
RIFT is built to catch that risk on the bench — before it costs years and dollars in the clinic.
Real-time In vitro Fluorescence Transcription — resolved molecule by molecule, not averaged from a population.
Cell-free, unlabeled, undisturbed.
Built to see the cross-reactivity that population averages erase.
Burst size, pausing, active promoters, captured as they happen.
Many compounds, run in parallel, at a fraction of the cost.
No lab build-out required — RIFT runs as an outsourced screen.
Partners send their compounds.
RIFT resolves each compound's effect on transcription, molecule by molecule.
Ranked by efficacy + cross-reactivity risk.
Advance the winners.
RIFT was invented in the Taatjes Lab — Enlixa is a CU Boulder spinout, grown from that research.


Biopharma, BD, or investors — tell us a little and we'll be in touch.
Running a transcription factor or chromatin regulator program? Reach out.
We'll get back to you shortly.