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M00324
CHO-K1/ADORA1/Gα15 Stable Cell Line
2 vials
Product Name CHO-K1/ADORA1/Gα15 Stable Cell Line
Full Name
Human Recombinant Adenosine A1 Receptor Stable Cell Line
Documents
Document-EXAMPLE: 11269_20091126015428.JPG (JPG)
TECHNICAL MANUAL: 11383_20091129194743.PDF (PDF)
Document-MSDS: 11422_20091130200610.PDF (PDF)
Figures
Reference
Species
Human
Description
A1 is a receptor for adenosine. It is demonstrated that the A1 receptor is ubiquitous throughout the entire body. Activation of A1 elicits an inhibition of adenylate cyclase and therefore a decrease in the cAMP concentration. A1 receptors are implicated in sleep promotion by inhibiting wake promoting cholinergic neurons in the basal forebrain. Adenosine antagonists are widely used in neonatal medicine.
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 ADORA1 receptor
Application Examples
Figure 1. NECA-induced concentration-dependent stimulation of intracellular calcium mobilization in CHO-K1/ADORA1/Gα15 and CHO-K1/Gα15 cells. The cells were loaded with Calcium-4 prior to stimulation with a ADORA1 receptor agonist, NECA. 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 NECA (Mean ± SD, n = 2). The EC50 of NECA on ADORA1 co-expressing with Gα15 in CHO-K1 cells was 84 nM. The S/B of NECA on ADORA1 co-expressing with Gα15 in CHO-K1 cells was 14.
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