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CHO-K1/Mouse β1-adrenoceptor Stable Cell

Item
Cat#
Price

Stable Cell Line

SNB-G-0028B

$19,800

Compound Testing Services

CT-001

$1,850 per 384w plate

(Up To 16 cpds Dose)


Product Description


The β1-adrenoceptor (beta-1 adrenergic receptor) is a G-protein-coupled receptor (GPCR) predominantly located in the heart and kidneys. It is the primary adrenergic receptor subtype in the heart, where its activation by catecholamines (e.g., noradrenaline, adrenaline) stimulates Gs-protein signaling, leading to increased heart rate (chronotropy), enhanced contractile force (inotropy), and accelerated conduction velocity (dromotropy). In the kidneys, β1-receptor activation stimulates the release of renin, thereby activating the renin-angiotensin-aldosterone system (RAAS).

Due to its crucial role in cardiac function, β1-adrenoceptors are a major therapeutic target.

 

Screeningbio’s CHO-K1/Mouse β1-adrenoceptor cell line overexpress Mouse ADRB1 and is designed to detect increases in intracellular cAMP levels in response to agonist stimulation of the receptor. Cisbio HTRF cAMP kit can be used to detect the signal. 

Product Specifications

Target Type

GPCR

Species

Mouse

HGNC Symbol

β1-adrenoceptor

Accession Number

NM_007419

Parental Line

CHO-K1

Lot#

See Vial

Storage

Liquid Nitrogen


Data

CHO-K1/Mouse β1-adrenoceptor Agonist Assay. CHO-K1/Mouse β1-adrenoceptor cells were treated with the reference agonist L-Adrenaline. 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.
CHO-K1/Mouse β1-adrenoceptor Agonist Assay. CHO-K1/Mouse β1-adrenoceptor cells were treated with the reference agonist L-Adrenaline. 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.



Target Background


The β1-adrenoceptor (beta-1 adrenergic receptor) is a G-protein-coupled receptor (GPCR) predominantly located in the heart and kidneys. It is the primary adrenergic receptor subtype in the heart, where its activation by catecholamines (e.g., noradrenaline, adrenaline) stimulates Gs-protein signaling, leading to increased heart rate (chronotropy), enhanced contractile force (inotropy), and accelerated conduction velocity (dromotropy).


In the kidneys, β1-receptor activation stimulates the release of renin, thereby activating the renin-angiotensin-aldosterone system (RAAS).

Due to its crucial role in cardiac function, β1-adrenoceptors are a major therapeutic target.


Product Documentation



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