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CHO-K1/Human SST3 Stable Cell

Item
Cat#
Price

Stable Cell Line

SNB-G-0214A

$19,800

Compound Testing Services

CT-001

$1,850 per 384w plate

(Up To 16 cpds Dose)


Product Description


The SST3 receptor (somatostatin receptor 3) is a member of the five-receptor family for somatostatin and is a prototypical Gi/o protein-coupled receptor. Its distribution in the human body is distinctive: within the central nervous system, it is selectively localized to the primary cilia of neurons in regions such as the cerebral cortex, hippocampus, amygdala, and hypothalamus; peripherally, it is expressed in the pancreas (pancreatic islet β-cells), the pituitary gland, and various neuroendocrine tumors. Its core function involves mediating the diverse biological effects of somatostatin by inhibiting adenylyl cyclase. It not only participates in regulating inter-neuronal signal transmission and cognitive memory processes but also induces cell cycle arrest and apoptosis in tumor cells, exerting anti-proliferative effects. Consequently, SST3 is consistently highly expressed in various tumors such as pituitary adenomas and thymomas, making it an important diagnostic marker and a potential therapeutic target.

 

Screeningbio’s CHO-K1/Human SST3 cell line overexpress SSTR3 and is designed to detect inhibition 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

Human

HGNC Symbol

SSTR3

Accession Number

NM_001051

Parental Line

CHO-K1

Lot#

See Vial

Storage

Liquid Nitrogen


Data

CHO-K1/Human SST3 Agonist Assay. CHO-K1/Human SST3 cells were stimulated with 2.5 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.
CHO-K1/Human SST3 Agonist Assay. CHO-K1/Human SST3 cells were stimulated with 2.5 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.


Target Background


The SST3 receptor (somatostatin receptor 3) is a member of the five-receptor family for somatostatin and is a prototypical Gi/o protein-coupled receptor.


Its distribution in the human body is distinctive: within the central nervous system, it is selectively localized to the primary cilia of neurons in regions such as the cerebral cortex, hippocampus, amygdala, and hypothalamus; peripherally, it is expressed in the pancreas (pancreatic islet β-cells), the pituitary gland, and various neuroendocrine tumors. Its core function involves mediating the diverse biological effects of somatostatin by inhibiting adenylyl cyclase. It not only participates in regulating inter-neuronal signal transmission and cognitive memory processes but also induces cell cycle arrest and apoptosis in tumor cells, exerting anti-proliferative effects.


Consequently, SST3 is consistently highly expressed in various tumors such as pituitary adenomas and thymomas, making it an important diagnostic marker and a potential therapeutic target.

Product Documentation



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