Lead Optimization

One of the most important steps in drug development, lead identification and optimization occurs on the resulting hit-to-lead high throughput screening experiments. During lead optimization, whether working on small molecule or biologics, efficacy and toxicity profiles of the target are critical. Pharmacokinetic and pharmacodynamic properties are assessed for small molecules during this phase.

Cell Line Development

biologics image under microscope

You can automate every step of the complex CLD workflow - from transfection to enrichment to limiting dilution to culture/feeding to assaying to hit picking and expansion.

Alleviate manual burden and reduce errors
Scheduling software ensures consistent plate treatment and tracks sample progress
Integrate multiple steps to automate the entire workflow

Absorption, Distribution, Metabolism & Excretion (ADME)

Tubes

Explore the effects a drug will have on the body.

Improve the consistency of your cell-based assays across experiments.
Reduce biological contamination
Integration of multiple systems ensures data integrity

Absorption, Distribution, Metabolism, Excretion & Toxicity (ADME-Tox)

Cell bank

ADME-Tox studies are crucial to ensure your drug candidates are characterized early on, and can reduce overall drug development costs significantly.

Identify which drugs will fail in the later stages of drug development, earlier.

Antibody Characterization and Sample Prep

Automate sample preparation for size, charge, sequence, glycosylation, and binding
Remove labor intensity and reduce error in your ELISAs
Sample preparation for proteomic and glycosylation analysis can be automated at varying throughput levels