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HEK293T/Rat V2 β-Arrestin Stable Cell

Item
Cat#
Price

Stable Cell Line

SNB-A-0227C

Inquiry

Compound Testing Services

CT-001

$1,850 per 384w plate

(Up To 16 cpds Dose)


Product Description


The V2 receptor (vasopressin V2 receptor) is a Gs protein-coupled receptor encoded by the AVPR2 gene, primarily distributed on the surface of renal collecting duct principal cells and vascular endothelial cells. Its core function, upon activation by arginine vasopressin, involves stimulating adenylyl cyclase via Gs protein to increase intracellular cAMP levels, thereby promoting the insertion of aquaporin-2 into the apical membrane of collecting ducts, enhancing water reabsorption to concentrate urine and maintain body water homeostasis. This receptor is the key molecule mediating antidiuretic effects; its gene mutations cause nephrogenic diabetes insipidus, and it serves as the primary target of clinical drugs (e.g., desmopressin) for treating diabetes insipidus and nocturnal enuresis.

 

ScreeningBio’s HEK293T/Rat V2 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

Rat

HGNC Symbol

AVPR2

Accession Number

NM_019136 (Rn)

Parental Line

HEK293T

Lot#

See Vial

Storage

Liquid Nitrogen


Data


HEK293T/Rat V2 β-arrestin Agonist Assay. HEK293T/Rat V2 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.
HEK293T/Rat V2 β-arrestin Agonist Assay. HEK293T/Rat V2 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.


Target Background


The V2 receptor (vasopressin V2 receptor) is a Gs protein-coupled receptor encoded by the AVPR2 gene, primarily distributed on the surface of renal collecting duct principal cells and vascular endothelial cells.


Its core function, upon activation by arginine vasopressin, involves stimulating adenylyl cyclase via Gs protein to increase intracellular cAMP levels, thereby promoting the insertion of aquaporin-2 into the apical membrane of collecting ducts, enhancing water reabsorption to concentrate urine and maintain body water homeostasis.


This receptor is the key molecule mediating antidiuretic effects; its gene mutations cause nephrogenic diabetes insipidus, and it serves as the primary target of clinical drugs (e.g., desmopressin) for treating diabetes insipidus and nocturnal enuresis.

 



Product Documentation



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