Glucagon GLP1R stably expressing cells
Tag-lite Glucagon GLP1 stably expressing cells
Over the past few years, SNAP-Tag technology combined with TR-FRET has paved the way for the development of many non-radioactive, no-wash, binding assays. The method is based on transfecting cells using plasmids encoding a SNAP-Tag and subsequently labeling them with Terbium. Cisbio offers a large collection of such plasmids. All GPCR genes are cloned in an expression vector directly downstream from a CMV promoter, and are provided ready for protein expression and labeling.
All information on this page pertains to the Tag-lite plasmid cloned with the GLP1 Glucagon receptor.
In collaboration with Boehringer Ingelheim - Présentations scientifiaues
In collaboration with Bayer - Présentations scientifiaues
Challenge the limits of binding kinetics studies - Notes d'application
The gold standard technology for receptor binding studies - Vidéos
Get the brochure about technology comparison. - Brochures
Available On-demand - Vidéos
How to revolutionize your kinetic binding demonstration with HTRF kinase binding platform assays - Notes d'application
Gene therapy processes: the significant advances, key facts and techniques - Infographies
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