
CHO-K1 Human CB1b β-Arrestin Stable Cell
Item | Cat# | Price |
Stable Cell Line | SNB-A-0048D | Inquiry |
Compound Testing Services | CT-001 | $1,850 per 384w plate (Up To 16 cpds Dose) |
Product Description
The CB1b receptor (cannabinoid receptor 1b) is a splice variant of the human cannabinoid receptor 1 (CB1), primarily distributed in peripheral metabolic tissues such as pancreatic β-cells and hepatocytes, with minimal expression in the brain. Its core function is to serve as a peripheral metabolic regulator, inhibiting adenylyl cyclase activity via Gi/o proteins to modulate insulin secretion and glucose metabolism, making it a potential drug target for metabolic disorders such as type 2 diabetes.
ScreeningBio’s CHO-K1/Human CB1b 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 | CNR1b |
Accession Number | NM_033181(Hs) |
Parental Line | CHO-K1 |
Lot# | See Vial |
Storage | Liquid Nitrogen |
Data
![CHO-K1/Human CB1b β-Arrestin Agonist Assay. CHO-K1/Human CB1b 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_e283e5c7957b42b99394326a921f7189~mv2.png/v1/fill/w_75,h_75,al_c,q_85,usm_0.66_1.00_0.01,blur_2,enc_auto/cbf7de_e283e5c7957b42b99394326a921f7189~mv2.png)
Target Background
The CB1b receptor (cannabinoid receptor 1b) is a splice variant of the human cannabinoid receptor 1 (CB1), primarily distributed in peripheral metabolic tissues such as pancreatic β-cells and hepatocytes, with minimal expression in the brain.
Its core function is to serve as a peripheral metabolic regulator, inhibiting adenylyl cyclase activity via Gi/o proteins to modulate insulin secretion and glucose metabolism, making it a potential drug target for metabolic disorders such as type 2 diabetes.
