

HEK293T/Human D3 β-Arrestin Stable Cell
Item | Cat# | Price |
Stable Cell Line | SNB-A-0084A | Inquiry |
Compound Testing Services | CT-001 | $1,850 per 384w plate (Up To 16 cpds Dose) |
Product Description
The dopamine D3 receptor is a member of the D2-like receptor subfamily and exhibits the highest affinity for dopamine among all dopamine receptors. Its distribution is notably restricted to the limbic system, with the highest density in the nucleus accumbens and olfactory tubercle, areas critical for emotion and reward. Functionally, the D3 receptor primarily modulates motivation, reward, cognition, and emotional processes and plays a central role in the reinforcing effects and drug-seeking behaviors of addiction. It is also implicated in the negative symptoms of schizophrenia (e.g., anhedonia, social withdrawal) and impulse control disorders associated with Parkinson's disease therapy. Consequently, selective D3 receptor ligands (e.g., partial agonists) are a major focus for developing new-generation antipsychotic and anti-addiction medications.
ScreeningBio’s HEK293T/Human D3 β-Arrestin cell line co-express the SmBiT tagged Human D3 receptor and the LgBiT tagged β-Arrestin. Activation of the GPCR-SmBiT induces β-Arrestin-LgBiT recruitment, forcing complementation of two NanoBiT enzyme fragments (SmBiT and LgBiT). The resulting functional NanoBiT enzyme catalyze substrate to generate a luminescent signal. Promega Nano-Glo Live Cell Kit can be used to detect the signal.
Product Specifications
Target Type | GPCR |
Species | Human |
HGNC Symbol | DRD3 |
Accession Number | NM_000796 (Hs) |
Parental Line | HEK293T |
Lot# | See Vial |
Storage | Liquid Nitrogen |
Data
![HEK293T/Human D3 β-Arrestin Agonist Assay. HEK293T/Human D3 β-Arrestin cells were treated with the reference agonist. Non-linear regression was used to plot activity changes vs. [Compound, M], and EC50 /IC50 values were determined, using GraphPad Prism software.](https://static.wixstatic.com/media/cbf7de_a32c63ab070646ce88935d597dea9e31~mv2.png/v1/fill/w_71,h_71,al_c,q_85,usm_0.66_1.00_0.01,blur_2,enc_auto/cbf7de_a32c63ab070646ce88935d597dea9e31~mv2.png)
Target Background
The dopamine D3 receptor is a member of the D2-like receptor subfamily and exhibits the highest affinity for dopamine among all dopamine receptors. Its distribution is notably restricted to the limbic system, with the highest density in the nucleus accumbens and olfactory tubercle, areas critical for emotion and reward.
Functionally, the D3 receptor primarily modulates motivation, reward, cognition, and emotional processes and plays a central role in the reinforcing effects and drug-seeking behaviors of addiction. It is also implicated in the negative symptoms of schizophrenia (e.g., anhedonia, social withdrawal) and impulse control disorders associated with Parkinson's disease therapy.
Consequently, selective D3 receptor ligands (e.g., partial agonists) are a major focus for developing new-generation antipsychotic and anti-addiction medications.