Hi everyone,
I am looking for some information regarding spinal cord sectioning to examine changes within the inhibitory interneuron population. I am used to sectioning brain tissue, but this will be my first time working with mouse spinal cord. Animals were perfused with 4% PFA and samples were left in PFA overnight. They are currently stored in PBS + 0.06% sodium azide. I usually put brain tissue in 30% sucrose 3-5 days before slicing...would I do the same for the spinal cord? Would the slicing protocol be similar for the spinal cord vs. brain tissue?
Any assistance is greatly appreciated! Thanks!