FIGURE SUMMARY
Title

Improved methods for marking active neuron populations

Authors
Moeyaert, B., Holt, G., Madangopal, R., Perez-Alvarez, A., Fearey, B.C., Trojanowski, N.F., Ledderose, J., Zolnik, T.A., Das, A., Patel, D., Brown, T.A., Sachdev, R.N.S., Eickholt, B.J., Larkum, M.E., Turrigiano, G.G., Dana, H., Gee, C.E., Oertner, T.G., Hope, B.T., Schreiter, E.R.
Source
Full text @ Nat. Commun.

In vivo characterization of CaMPARI2 in zebrafish. a Representative z-projection from a confocal stack from a 6-dpf larval transgenic pan-neuronal CaMPARI2 zebrafish brain photoconverted for 30 s during free swimming. b Boxplots represent the distribution of red-to-green fluorescence signals from individual neurons (between 1800 and 6000 cells per condition, representing 2–4 fish (Supplementary Fig. 9, 10). Data are measured from neurons in the forebrain (white box in a) following photoconversion of either freely swimming or tricaine-anesthetized larval zebrafish. Box represents 1st, 2nd, and 3rd quartile, while whiskers represent the 5th and 95th percentile. Scale bar is 100 µm

Acknowledgments
This image is the copyrighted work of the attributed author or publisher, and ZFIN has permission only to display this image to its users. Additional permissions should be obtained from the applicable author or publisher of the image. Full text @ Nat. Commun.