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首頁 /藥靶模型 /GPCR靶點細胞 /Class A(Rhodopsin) /CB1/β-Arrestin/CHO

CB1/β-Arrestin/CHO

CBP71391

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I. Background
The cannabinoid receptor CNR1 is Gs-coupled GPCRs expressed in primarily CNS and some peripheral neurones; particularly prevalent in basal ganglia, hippocampus, cerebellum, cerebral cortex and also presented in some non-neuronal cells and tissues, for example leukocytes and testis. A shorter human splice variant (411aa) has been identified in the brain and other tissues by reverse-transcriptase PCR but mRNA levels were less than 10-fold the levels of the longer isoform. The pharmacological characteristics of the isoforms are similar.
 
II. Introduction
Host Cell:

CHO

Stability: 20 passages (in-house test, that not means the cell line will be instable beyond the passages we tested.)
Freeze Medium: 90% FBS+10% DMSO
Culture Medium: F12k+10%FBS+5ug/ml puromycin+5ug/ml blasticidin
Mycoplasma Status: Negative
Storage: Liquid nitrogen immediately upon delivery
Application(s): Functional assay for CNR1
Transducer: β-Arrestin
 
Ⅲ. Description of Host Cell Line
Organism: Hamster
Tissue: Ovary
Morphology: Epithelial
Growth Properties: Adherent
 
Ⅳ. Representative Data

Figure 1. Recombinant CB1/β-Arrestin/CHO constitutively expressing CB1.

Figure 2.Dose response of CP-55940 in CB1 β-Arrestin CHO-K1 Cell Line (C2)

Figure 3.Inhibition of CP-55940-induced Beta-Arrestin Recruitment in CB1 Beta-Arrestin CHO-K1 Cells (C2).


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