Human CHO-K1/SST5/Gα15 Stable Cell Line

[CAT#: NCL20120128CR]

SST5 Somatostatin Receptor Stable Cell Line

Species:: Human

Applications:: GPCR Screening

Cell Types:: Other Cells

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Product Overview

Description

SSTRs are widely expressed in many tissues, frequently as multiple subtypes that coexist in the same cell. With expressions in a tissue-specific manner, SSTRs are involved in the regulation of secretion of insulin, glucagon and growth hormone as well as cell growth induced by neuronal excitation in both the central and peripheral nervous systems.

Cell Types

Other Cells

Applications

GPCR Screening

Research Areas

GPCR; Neural Cell

Species

Human

Properties

Size

>1x10^6 Cells

Form

Frozen cells

Culture Medium

Ham's F12, 10% FBS, 100 μg/ml Hygromycin B, 200 μg/ml Zeocin

Freeze Medium

45% culture medium, 45% FBS, 10% DMSO

Receptor

SST5/SSTR5

Family

Somatostatin receptor

Strain

SST5/Gα15 Cell Line

Cell Purity

>95%

Shipping

Dry ice

Storage

Liquid nitrogen immediately upon delivery

Handling Advice

Avoid inhalation. Avoid contact with eyes, skin, and clothing. Avoid prolonged or
repeated exposure.

Research Use Only

For research use only, not for diagnostic or therapeutic use.

Warnings

Store under recommended storage conditions (liquid nitrogen). Do not expose to high temperature. After expiration, discard all remaining reagents.

Target Details

Target

SST5

Official Name

SST5

Alternative Names

sst5 receptor; SSTR5; SRIF1; SRIF1B; SOMATO; Smstr5; SS-5-R; SS5-R; SS5R; Somatostatin receptor subtype 5; somatostatin receptor type 5; sst5

References

1. Jamal-Livani, N., Mohammadian, E., Arabi, M. S., & Safdari, Y. (2020). Protein-based drug carrier specific for HER2-positive breast cancer cells. Journal of Drug Delivery Science and Technology, 101623. 2. Rebois, R. V., Maki, K., Meeks, J. A., Fishman, P. H., Hébert, T. E., & Northup, J. K. (2012). D2-like dopamine and β-adrenergic receptors form a signaling complex that integrates Gs-and Gi-mediated regulation of adenylyl cyclase. Cellular signalling, 24(11), 2051-2060.

Publications