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M00290
CHO-K1/OPRK1/Gα15 Stable Cell Line
2 vials
Product Name CHO-K1/OPRK1/Gα15 Stable Cell Line
Full Name
Human Recombinant κ-Opioid Receptor OPRK1 Stable Cell Line
Documents
TECHNICAL MANUAL: 11187_20091030030646.PDF (PDF)
Document-EXAMPLE: 11189_20091030030815.JPG (JPG)
Document-MSDS: 11427_20091130202048.PDF (PDF)
Figures
Reference
Species
Human
Description
Opioid receptors and their endogenous peptide ligands play important roles in the reward and reinforcement of drugs such as heroin, cocaine, and alcohol. The κ-opioid receptor is a type of opioid receptor which binds the peptide opioid dynorphin as the primary endogenous ligand. κ-opioid receptors are widely distributed in the brain, spinal cord, and in pain neurons. They are associated with the risk for alcohol dependence.
Freeze Medium
45% culture medium, 45% FBS, 10% DMSO
Culture Medium
Ham's F12, 10% FBS, 100 μg/ml Hygromycin B, 200 μg/ml Zeocin
Storage
Liquid nitrogen immediately upon delivery.
Application
Functional assay for OPRK1 receptor
Application Examples
Figure 1. U-50488-induced concentration-dependent stimulation of intracellular calcium mobilization in CHO-K1/OPRK1/Gα15 and CHO-K1/Gα15 cells. The cells were loaded with Calcium-4 prior to stimulation with a OPRK1 receptor agonist, U-50488. The intracellular calcium change was measured by FlexStation. The relative fluorescent units (RFU) were plotted against the log of the cumulative doses (10-fold dilution) of U-50488 (Mean ± SD, n = 2). The EC50 of U-50488 on OPRK1 co-expressing with Gα15 in CHO-K1 cells was 4.7 nM. The S/B of U-50488 on OPRK1 co-expressing with Gα15 in CHO-K1 cells was 24.
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