Hi,

I have IHC staining on 2-3 serial FFPE tissue sections. I did my best to take pictures of the same regions on a brightfield microscope but I'd like to be able to align each section into a single overlay/stack (kind of like a z-stack) at the resolution of hematoxylin-stained nucleiii. Does anyone have any tips on how to do this somewhat easily in Image J/Fiji? Thank you in advance for your help!

Best

Adam

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