Dissociated cells labelled with GAP-Cherry or GAP-YFP were mixed and plated on glass bottom dish containing 1×MBS-H. Images were acquired using a Quorum technologies WaveFX spinning disc confocal mounted on an automated DMI6000B Leica microscope, with a 40x HCX PL APO CS, NA = 1.25 oil objective was used. Overall, 491 and 561 nm diode lasers were used for GFP and Cherry excitation, respectively. Images were collected with EM CCD 512X512 BT camera using the acquisition software Improvision Volocity 3DM.
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