Hello,
I have a z-stack acquired on a Zeiss LSM 510 META confocal of a sample in 2 channels (single time point). I would like to be able to extract x-z and y-z slices so that I can analyse the fluorescence intensity across them. Is this possible and/or does anyone know how to do this in ImageJ?
Thanks in advance for your help,
Graham
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Graham Wright
Microscopy & Imaging Facility
Temasek Life Sciences Laboratory
1 Research Link
National University of Singapore
Singapore 117604
P: +65 6872 8406
M: +65 8256 7916
E:
[hidden email]