Pre-defined and Custom Assay Development
Our assay development and screening biologists combine target class and cell biology expertise with state-of-the-art instrumentation to provide services tailored to your requirements. We provide a collaborative environment and work closely with our teams in medicinal chemistry, ADME, structural biology and fragment-based drug discovery to deliver within challenging timelines.
American College of Toxicology (ACT) Annual Meeting
In case you missed any of these presentations at ACT and wonder if they’re available on demand, the answer is Simply, Yes. Explore our resources to download presentations, poster recordings, and other content from ACT.
Factors to Consider for Assay Development
A well-designed assay takes many factors into consideration. For example, assays that work well in small batches may not be scalable; compounds and reagents can be difficult to obtain; and perhaps worst of all, false positives and negatives can shift the focus away from relevant hits. Are you prepared to address these issues? Take a look:
Stability with time
Stability of expression (for cellular targets)
|Control compounds/conditions||Are they available?
Are they valid?
|Assay robustness||Appropriate pharmacology
Z’ ‐factor & signal window (under valid control conditions)
|Assay format||384 or 1536-well
Reagent availability and cost
False positive liability
|Confidence in hits and hit rate||False positive and false negative rates
Predicted activity threshold and hit rate
Positional effects on data distribution
|Automation||Can the assay be scaled?
Liquid handling considerations
Liquid handler quality control (QC) interval
|Data handling||Processing volume of data
|Hit progression||Orthogonal assays
Our scientists are skilled at evaluating clients’ pre-defined assays, are able to make recommendations, and can create custom solutions that overcome some of the challenges of assay design.
Flexible Schedule and Price Structure
Charles River’s assay development and screening services are designed to meet your budget and timeline. Prior to the launch of any campaign, we meet with you to fully understand your project’s starting point, scope, and objectives and recommend the best course of action. Our standard fee-for-service contract maximizes budget and minimizes time for projects with a well-defined scope.
Alternatively, our full-time equivalent (FTE) option is available if you need additional services such as target validation, exploration of feasibility, or execution of multiple assays. In this model, we designate an experienced alliance manager to serve as your single point of contact for scientific direction, resource prioritization, and project scheduling.
Assay Development Frequently Asked Questions (FAQs)
Do you perform custom assay development?
Yes, about 40% of screens that we perform are developed first at Charles River. We have highly experienced assay development teams with a broad and diverse screening technology base.
- What is your range of compound target classes?
I’m interested in transferring my assay. Can I leverage your assay screening services?
Yes. Many of our clients choose to transfer their assays. Our team carefully evaluates and validates pre-defined assays against all design criteria to make sure the study is feasible for the desired target, consistently reliable, and scalable to automation to ensure optimum results.
- What types of compound libraries do you offer?