Hi,
I acquired multiple confocal stack images of olfactory epithelium from rostral to caudal position from 1 slide. I want to create 3d reconstruction by adding all the z stacks to look at expression pattern of few neuronal markers. I am able to add multiple stacks by selecting "add slice" option. However, there is a distance of 50 micron between every 2 slices. 2 questions:
1) Can I add blank space of 50 micron between every 2 slices?
2) How to align for x-y drift between different z stacks?
Thank you
Raghu