01Review the evidence
Assess existing protocols, performance data, reagents and the intended use to identify likely sources of variability.
A focused investigation into the factors limiting sensitivity, specificity or consistency, followed by practical, evidence-led improvements.
Assess existing protocols, performance data, reagents and the intended use to identify likely sources of variability.
Prioritise a small set of variables and measurable acceptance criteria before starting bench work.
Study reagent loading, buffers, blocking, reaction conditions or sample handling as appropriate to the platform.
Compare the revised workflow with the baseline and document remaining limitations and next steps.
When an assay is partly working, the fastest useful step is often a focused comparison against the current protocol. We review existing data, identify the variables most likely to limit performance and agree how improvements will be measured.
Usually we begin with your current reagents, protocol and data. The scope can focus on the specific bottleneck instead of repeating the whole development process.
Measures depend on the assay and project, but may include detection range, background, recovery, precision, matrix effects and run-to-run variation.
Share your assay requirements or formulation goals and current stage. We'll discuss how to structure the next step.
Start a conversation