Fig. 2
From: Improved methods for marking active neuron populations

Brightness and photoconversion of CaMPARI1 and CaMPARI2. Two-photon images of CaMPARI1 and CaMPARI2_F391W-L398V (no epitope tags) expressed in CA1 neurons of rat hippocampal slice cultures before and after pairing of stimulation (100 bAPs at 100 Hz) with UV light (2 s, 16 mW mm−2). Two lasers were simultaneously employed to acquire images of the green (980 nm) and red species (1040 nm) of the CaMPARI variants. A single cell, denoted by a pipette drawing, is patched and stimulated during the UV illumination. Green and red fluorescence is quantified along with the fold R/G in both stimulated (CaMPARI1 n = 5; CaMPARI2 n = 6) and unstimulated neighboring neurons (CaMPARI1 n = 5; CaMPARI2 n = 14) as a function of the number of pairings. Error bars are SEM. Note that fluorescence intensity is normalized to the laser power (see Methods), showing the increased brightness of CaMPARI2. Scale bars are 25 µm