Dopamine D2 and D3aR fluorescent probe
Tag-lite Dopamine D2 & D3a receptors 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 D2 Dopamine type 2 receptor.
In collaboration with Boehringer Ingelheim - Scientific Presentations
In collaboration with Bayer - Scientific Presentations
Challenge the limits of binding kinetics studies - Application Notes
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The gold standard technology for receptor binding studies - Videos
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Available On-demand - Videos
How to revolutionize your kinetic binding demonstration with HTRF kinase binding platform assays - Application Notes
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