

CHO-K1/Human C5A2 β-Arrestin Stable Cell
Item | Cat# | Price |
Stable Cell Line | SNB-A-0079D | Inquiry |
Compound Testing Services | CT-001 | $1,850 per 384w plate (Up To 16 cpds Dose) |
Product Description
The complement C5a receptor 2 (C5AR2, also known as C5L2) is another G protein-coupled receptor for C5a. It shares a similar distribution pattern with C5AR1 (e.g., neutrophils, monocytes, adipocytes) but lacks typical chemotactic functions. It is primarily regarded as a "decoy/modulatory receptor," regulating C5AR1 signaling and ligand internalization by binding with high affinity to both C5a and its metabolite C5a des-Arg. It also influences energy metabolism, playing a complex role in the regulatory networks of inflammatory and metabolic diseases.
ScreeningBio’s human C5A2 β-arrestin cell line is an ideal tool for studying GPCR/β-arrestin interactions. In this system, the GPCR C-terminus is fused to a smallBiT tag, and the β2-arrestin N-terminus is fused to a largeBiT tag. Upon receptor activation, GPCR/β-arrestin interaction brings the two fragments together to reconstitute an active NanoLuc enzyme, which can be quantified using the NanoBiT substrate. This cell line is designed to evaluate a compound’s ability to activate the β-arrestin signaling pathway.
Product Specifications
Target Type | GPCR |
Species | Human |
HGNC Symbol | C5AR2 |
Accession Number | NM_018485 (Hs) |
Parental Line | CHO-K1 |
Lot# | See Vial |
Storage | Liquid Nitrogen |
Data
![CHO-K1/Human C5A2 β-Arrestin Agonist Assay. CHO-K1/Human C5A2 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_75fdf218cc3e424393740fc3fde12415~mv2.png/v1/fill/w_75,h_75,al_c,q_85,usm_0.66_1.00_0.01,blur_2,enc_auto/cbf7de_75fdf218cc3e424393740fc3fde12415~mv2.png)
Target Background
The complement C5a receptor 2 (C5AR2, also known as C5L2) is another G protein-coupled receptor for C5a. It shares a similar distribution pattern with C5AR1 (e.g., neutrophils, monocytes, adipocytes) but lacks typical chemotactic functions.
It is primarily regarded as a "decoy/modulatory receptor," regulating C5AR1 signaling and ligand internalization by binding with high affinity to both C5a and its metabolite C5a des-Arg.
It also influences energy metabolism, playing a complex role in the regulatory networks of inflammatory and metabolic diseases.