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CHO-K1/Human CB1b Stable Cell

Item
Cat#
Price

Stable Cell Line

SNB-G-0048D

$19,800

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 cell line overexpress human CB1b and is designed to detect inhibition in intracellular cAMP levels in response to agonist stimulation of the receptor. HTRF cAMP kit can be used to detect the signal.

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 Agonist Assay. CHO-K1/Human CB1b cells were stimulated with 5 μM Forskolin and treated with reference agonist. The assay was run based on Revvity cAMP HTRF protocol. Non-linear regression was used to plot activity changes vs. [Compound, M], and EC50 values were determined, using GraphPad Prism software.C
CHO-K1/Human CB1b Agonist Assay. CHO-K1/Human CB1b cells were stimulated with 5 μM Forskolin and treated with reference agonist. The assay was run based on Revvity cAMP HTRF protocol. Non-linear regression was used to plot activity changes vs. [Compound, M], and EC50 values were determined, using GraphPad Prism software.C


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.

Product Documentation



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