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  • A robust and Efficient FRET-Based Assay for Cannabinoid Receptor Ligands Discovery.

    New scaffolds modulating the CBRs in both the orthosteric and allosteric sites have been developed, supported by resolved crystal structures of both CBRs.[4–8] A key challenge in CBR modulator development is separating can be appreciated when talking about SCRAs (Synthetic Cannabinoid Agonists), as one of the series developed Results 2.1  CELT-335 Binding at CB1 and CB2 Receptors The first step for the development of the assay Using these results as a starting point, the Tag-lite® binding assay was developed.

  • High-Content Screening for GPCR Programs: Overcoming Assay Limitations with Fluorescent Ligands

    GPCR-focused programs, the ability to visualize receptor localization, internalization kinetics, and ligand For GPCR assay developers, HCS supports:  Quantitative visualization of receptor internalization and How Fluorescent Ligands Strengthen HCS Assays: The Case of CELT-331 Fluorescent ligands are now considered information that clarifies receptor behavior under different ligand conditions. technologies without needing internal imaging infrastructure or specialized assay development expertise

  • Optimizing HTRF Assays with Fluorescent Ligands: Time-Resolved Fluorescence in GPCR Research

    physiological processes, making them a key target in drug development.   This also improves detection of low affinity or slow binding ligands. In a recent study , we contributed to the development of a robust HTRF assay for the discovery of new A Robust and Efficient FRET-Based Assay for Cannabinoid Receptor Ligands Discovery. By combining deep expertise in GPCR biology with advanced fluorescence chemistry, Celtarys custom-developed

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