The Tag-lite 5HT1A 5-Hydroxytryptamine 1A plasmid is used to transiently or stably transfect cells for the purpose of developing a 5HT1A 5-Hydroxytryptamine 1Areceptor binding assay.
For research use only. Not for use in diagnostic procedures.
Feature | Specification |
---|---|
Application | Receptor-Ligand Binding |
The Tag-lite 5HT1A 5-Hydroxytryptamine 1A plasmid is used to transiently or stably transfect cells for the purpose of developing a 5HT1A 5-Hydroxytryptamine 1Areceptor binding assay.
For research use only. Not for use in diagnostic procedures.
Over past few years, SNAP-Tag technology combined with TR-FRET has paved way development of many non-radioactive, no-wash, binding assays. method is based on transfecting cells using plasmids encoding a SNAP-Tag and subsequently labeling m with Terbium. Revvity 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 protein expression and labeling.
All information on this page pertains to Tag-lite plasmid cloned with 5HT1A 5-Hydroxytryptamine 1A receptor.
Application |
Receptor-Ligand Binding
|
---|---|
Brand |
Tag-lite
|
Detection Modality |
HTRF
|
Product Group |
Plasmids
|
Shipping Conditions |
Shipped in Dry Ice
|
Target Class |
GPCR
|
Technology |
TR-FRET
|
Therapeutic Area |
Cardiovascular
Infectious Diseases
Metabolism/Diabetes
NASH/Fibrosis
Neuroscience
Oncology & Inflammation
Rare Diseases
|
Unit Size |
1 Item
|
Use standard transfection techniques (refer to transient transfection protocol) to transiently express the SNAP-GPCR of interest in your cell line.
SNAP-tag®, is a small fusion tag that covalently interacts with specific substrates. SNAP-tag allows specific and covalent labeling of any protein of interest (refer to labeling procedure). Cells are provided unlabeled and need to be labeled with Lumi4-Terbium prior to running a binding assay. Labeling reagents are available from the Revvity catalog in 4 different sizes.
Running a receptor binding assay using Tag-lite is as easy as it can get. Simply dispense 10 µL of labeled cells into each well, followed by 5 µL of labeled ligand and 5 µL of the compound you wish to test. Like all HTRF assays, Tag-lite assays do not require any washing steps. A diagram of the procedure to be followed is given on the right.
A saturation binding assay measures total and non-specific binding for increasing concentrations of ligand under equilibrium conditions. To perform the assay, the fluorescent ligand is titrated into a solution containing a fixed amount of labeled cells and then incubated to equilibrium. The HTRF ratio obtained from this titration is the total binding.
A competitive binding assay is performed to measure the dissociation constant, Ki. To perform the assay, the compound is titrated into a solution containing a fixed concentration of fluorescent ligand and a fixed amount of cells.
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G-protein coupled receptors (GPCRs) are crucial transmembrane proteins involved in cellular signal transduction.
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