At SYG BIOTECH, we develop cutting-edge solutions for the discovery and analysis of therapeutic proteins, enabling breakthroughs in oncology and beyond. In this post, we showcase our cost-effective in vitro PD-1 PD-L1 blockade assay that can be utilized to obtain quick, but essential potency in vitro data prior to progressing to in vivo animal pharmacology, toxicology and/or efficacy studies.
Optimized for PD-1/PD-L1 Pathway Targeting: This assay is ideal for evaluating antibodies, Fc-fusion proteins, small molecule antagonists, and other biologics designed to inhibit the PD-1/PD-L1 interaction. It provides a robust and reliable platform for screening and characterizing therapeutic candidates with high sensitivity and specificity.
Seamlessly integrate the PD-1/PD-L1 blockade assay into your lead compound screening program to accelerate the identification of promising therapeutic candidates in early drug discovery. Conduct high-throughput testing of novel compounds without the need for animal models, ensuring efficiency and ethical research practices.
Our PD-1/PD-L1 blockade assay precisely evaluates the potency of your antibody, enabling accurate EC50 value determination. In this assay, bioluminescence directly correlates with compound potency, providing a predictive basis for in vivo efficacy—crucial for informed therapeutic development.
Assessing the interaction of a specific ligand with its target protein often involves expensive, time-consuming, and labor-intensive methods that require specialized equipment and expertise. In contrast, our method provides a cost-effective and user-friendly alternative to the traditional techniques. Protocols can be adapted to a wide range of research questions.
Join us as we set new standards in biotechnology and unlock the potential of personalized medicine.