Product Description |
Recombinant CHO-K1 cells stably overexpress human adenosine A2A receptor (ADORA2A) on the surface and contain high levels of G protein Gαs to couple with the receptor in downstream signaling pathways. |
Culture Properties |
Adherent |
Stability |
Stable through more than 16 passages with no significant changes in assay performance or expression profile. |
Size |
Two vials of frozen cells (>1×106 per vial in 1 mL) |
Storage |
Store cells in liquid nitrogen immediately upon receipt. Thaw and recover cells within one year from the date received. |
Culture Medium |
Ham’s F-12K (Kaighn’s), 10% FBS, 200 μg/ml Zeocin (Cat. No. R250-01, Life Technologies), 100 μg/ml Hygromycin B (Cat. No. 10687010, Life Technologies) |
Complete Growth Medium |
Ham’s F-12K (Kaighn’s), 10% FBS |
Freeze Medium-DATA |
45% Ham’s F-12K (Kaighn’s) (Cat. No. 21127, Life Technologies), 45% FBS (Cat. No. 10099-141, Life Technologies), 10% DMSO (Cat. No. D2650, Sigma) |

Figure 1. Dose dependent stimulation of intracellular cAMP accumulation upon treatment with NECA in CHO-K1/ADORA2A/Gα15 cells. d2 acceptor fluorophore -labeled cAMP (Cat. No. 62AM4PEC; Revvity) and intracellular cAMP in CHO-K1/ADORA2A/Gα15 cells competitively bind with Europium Cryptate-labeled anti-cAMP monoclonal antibody. The FRET signal decreases as the intracellular cAMP concentration rises and was measured by plate reader (Pherastar, BMG). The EC50 of NECA on CHO-K1/ADORA2A/Gα15 cells was 2.01 nM.
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use.
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