Hi, I am trying to analyze Golgi organization in neurons. I’ll appreciate if you could let me the best way to analyze the morphology/changes in Golgi in neurons. We are trying to analyze Golgi phenotypes (fragmented, diffused or condensed) in different groups of neurons. We have stained cultured neurons with GM130 and TGN38. Are there any tools in Image-J by which we can define the different pattern of shape and distribution pattern of Golgi inside cultured neurons? Thank you.