Custom services
Move from a scientific need to a dependable assay
Work with our development scientists to turn a research method into a reproducible, documented assay that holds up across operators, sites and sample types.
What this covers
How assay development works with us
- Feasibility assessment against your sample type and readout
- Optimisation of chemistry, cycling and detection conditions
- Reproducibility and robustness testing before handover
At a glance
- Typical scope
- Feasibility to validated protocol
- Sample types
- FFPE, blood, cells, tissue, purified nucleic acid
- Readouts
- qPCR, dPCR, NGS, immunoassay
- Deliverables
- Protocol, validation summary, reagent list
Service flow
- 1Define the question
- 2Build and test
- 3Validate
- 4Transfer
Process
A clear path from enquiry to delivery
- Step 01
Define the question
We review your sample, target and required sensitivity together.
- Step 02
Build and test
Iterative optimisation with clear, agreed acceptance criteria.
- Step 03
Validate
Reproducibility, robustness and interference checks.
- Step 04
Transfer
Documented protocol and reagent supply plan for routine use.
Good to know
Development projects are scoped after a short technical call — no commitment is needed to review feasibility.
Talk to us
Tell us what you need and we will scope it with you
Share the essentials and a specialist from the relevant team will respond with next steps, feasibility and indicative timing.
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Not sure which service fits your project?
Our scientists can help you choose between custom development, formatting and manufacturing support.
