Lean, agile micro-CRO (Contract Research Organization) rescuing underperforming ELISAs and kits for higher S/N, wider dynamic range, and a fully documented handoff.
Optimization of antibody pairs, buffers, and incubation times to meet your target S/N, %CV, and dynamic range, whether you are starting from a commercial kit or a fully custom assay concept.
Fully supported assay transfer with side-by-side runs against pre-defined acceptance criteria. Includes handoff-ready protocol and development report.
Rigorous testing in your specific sample matrix (e.g., serum, plasma, lysate). We characterize parallelism, linearity, and spike-recovery to ensure real-world accuracy.
Optimization for cell-based or homogeneous readouts (e.g., HTRF, reporter assays). We establish stable protocols for lysate or live-cell quantification.
New: White paper on MOA-aligned cytokine-release potency assays → Read now
Step 1
Define project scope, sample matrix, and target acceptance criteria.
Step 2
Execute simple CDA and coordinate shipment of samples & critical reagents.
Step 3
Factorial screen to identify critical parameters (e.g., buffers, antibody concentration, incubation).
Step 4
Refine protocol to tighten %CV, widen dynamic range, and confirm LoD/LoQ.
Step 5
Deliver final protocol, development report, and raw data; includes a scientific debrief call.
A: We are built for a different purpose. Our “micro-CRO” model provides two key advantages:
We operate RUO‑only with GLP‑lite QC for R&D decision‑making. For regulated studies, we provide technology transfer documentation and support back to your GLP/GMP labs.
We propose a timeline during the fit call; simple tune‑ups often begin within days of material receipt.
A comprehensive mutual CDA available. We follow strict sample handling and data privacy practices; only assigned scientists access your data. We anonymize samples through our internal tracking system.
Direct, Indirect, Competitive, Sandwich, ELISpot.
Cell based assays, binding kinetics (SPR), affinity & potency.
Colorimetric, fluorescent, luminescent, FRET/HTRF.
Commercially-available primary cells and immortalized mammalian cells: both adherent and suspension. Â
A simple 4-5 step workflow:
Consult → intake → design → run → deliverable.
Standard ELISA work:Â Standard samples run on an existing ELISA kit can start as low as $1,000 per run, with an additional $200 per plate.
ELISA Creation and Development Work: Pilot runs (assay creation and development pilots) start at $1,800 and decrease marginal cost depending on volume and number of runs. This cost considers the additional time required for custom projects when planning, analyzing, and reporting.
Additional services:Â Â
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Additional Fees:  Our set-up fee for new projects is typically $1,000. This includes client on-boarding, technology and data transfer, sample ingestion, and overall project management. This can go as low as $400 for particularly straightforward projects. Passthrough pricing is the most typical arrangement for materials cost, where we will purchase the reagents required, to be reimbursed by the clients at project termination. Development reports are often included for basic projects. All of your raw and analyzed data, the final developed protocol(s), and a smile are always offered for free.
We typically estimate about 15 minutes for introductory calls but set aside 30 minutes to ensure ample time to discuss all your needs.
All consultations are confidential and commitment-free.
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Drop a question and we’ll get back to you.
RUO only. No diagnostic claims. Confidential by default; mutual CDA available.
Prefer to skim first?  Read our white paper →