Immunolabeling methods to analyze distinct populations of microtubules in the developing zebrafish brain are described here, which are broadly applicable to other tissues. The first protocol outlines an optimized method for immunolabeling stable and dynamic microtubules. The second protocol provides a method to image and quantify nascent microtubules specifically.
McFarland, R. J., Brown, S. P., Vital, E., Werner, J. M., Brewster, R. M. Use of Immunolabeling to Analyze Stable, Dynamic, and Nascent Microtubules in the Zebrafish Embryo. J. Vis. Exp. (127), e55792, doi:10.3791/55792 (2017).