GIPR fluorescent probe
Tag-lite GIP receptor fluorescent probe
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 GIPR Glucagon receptor.
In collaboration with Boehringer Ingelheim - Scientific Presentations
In collaboration with Bayer - Scientific Presentations
Challenge the limits of binding kinetics studies - Application Notes
The gold standard technology for receptor binding studies - Videos
Get the brochure about technology comparison. - Brochures
Available On-demand - Videos
How to revolutionize your kinetic binding demonstration with HTRF kinase binding platform assays - Application Notes
Choosing the right microplate reader ensures you’ll get an optimal readout. Discover our high performance reader, or verify if your lab equipment is going to be compatible with this detection technology.Let's find your reader