Biological Information | |
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Background Information: | The PathHunter® rDRD2S cell line is a stable, engineered cell line for use in studying drug candidates (small molecules or biologics) targeting GPCRs. This cell line enables assessment of ligand (e.g. dopamine) based activation of rDRD2S GPCR activity via detection of β-arrestin recruitment. This product uses EFC technology. The included cell line overexpresses PK-tagged rDRD2S and EA-tagged β-Arrestin 2. Activation of rDRD2S stimulates the recruitment of β-Arrestin 2 and produces EFC signal. This stable modified cell line is provided as two vials of cryopreserved cells. Please note that this product expresses the rat version of this protein. |
Target Class: | GPCR |
Family: | Dopamine Receptors |
Coupling: | Gi/Go |
Accession Number: | M36831 |
Target Name: | DRD2 (S) |
Target Aliases: | Dopamine Receptor D2 (short isoform), D2DR, D2R |
Target Species: | Rat |
Cell Background: | CHO-K1 |
Usage | |
Product Type: | Stable Cell Lines |
Application: | Drug Discovery & Development |
Storage Conditions: | Store in vapor phase of liquid nitrogen. |
Usage Disclaimer: | These products may be covered by issued US and/or foreign patents, patent application and subject to Limited Use Label License. Please visit discoverx.com/license for a list of products that are governed by limited use label license terms and relevant patent and trademark information. |
Assay Information | |
Assay Type: | Functional |
β-Arrestin isoform: | β-Arrestin-2 |
Assay Measures: | β-Arrestin Recruitment |
Detection Method: | Chemiluminescence |
Additional Information | |
Brand: | PathHunter® |
PathHunter® CHO-K1 rDRD2S (Short Isoform) β-Arrestin Cell Line
The PathHunter® CHO-K1 rDRD2S (Short Isoform) β-Arrestin Cell Line measures rDRD2S (GPCR) activity via recruitment of β-Arrestin2. This cell line ships as two vials of cryopreserved cells. Rat protein.
User Manuals & Protocols
70-247 PathHunter Beta-Arrestin Assay for GPCR Cell Lines REV5 User Manual
View DocumentDatasheets
93-0778C2 Datasheet
View Document