Kinases are vital regulators of cellular signalling and important therapeutic research targets. Our kinase panels support early drug discovery by helping identify and evaluate the potential of kinase inhibitors, with a range of panel formats designed for diverse research needs.
Focused CDK panel for cell-cycle and transcriptional regulation research.
Tyrosine kinase-focused panel for signal-transduction and oncology research.
Economical, rapid and efficient screening focused on core wild-type kinases.
A broad spectrum of wild-type kinases for comprehensive profiling studies.
The most comprehensive panel, covering human-origin wild-type and mutant kinases.
A broad spectrum of kinase targets supports thorough analysis and evaluation.
HTRF and ADP-Glo platforms deliver precise, reproducible and rapid kinase activity measurements with flexible configurations for diverse research needs.
For selected kinases, assays can be performed under 1 mM ATP conditions to provide enhanced physiological relevance and more predictive insight into compound efficacy.
Our experienced team delivers accuracy, consistency and insightful interpretation in functional kinase profiling.
Reference data can help illustrate compound activity across kinase families, supporting the early identification of selectivity profiles and potential off-target effects.

This kinase inhibition dendrogram illustrates the inhibitory efficacy of BI-3406 at 1 µM across a spectrum of kinase families. Kinases are grouped by phylogenetic relationship, including TK, CMGC, AGC, CAMK, CK1, STE and TKL.
Each kinase is marked with a dot, with colour indicating inhibition: red, 90–100%; yellow, 80–90%; blue, 70–80%; light blue, 50–70%; and green, below 50%. This visualization helps identify selectivity profiles, potential therapeutic targets and possible off-target effects relevant to drug development and safety assessment.
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