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Assessment of CB2 receptor function in the absence and presence of GPR55 using label-free DMR technology. All stable cell lines were stimulated with 1 μM of the mixed CB1/CB2 receptor agonist, 2-AG, or DMSO as vehicle and the resulting picometer shifts of reflected light wavelength were monitored over time as in Figure 7. Shown are mean values ± SEM of one out of four independent experiments each performed in triplicate.
