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A query regarding post-fixation (for immunofluorescence)

immunofluorescence fixation

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#1 KRN

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Posted 02 February 2012 - 11:51 AM

Hi all,

I am trying to measure c-Fos expression in free floating brain sections using immunofluorescence. For some reason, I don't see the c-Fos in the nucleus. I see it mostly in the cytosol and dendrites. In addition, the signal to noise ratio is pretty bad..

I have managed to focus the problem on the post-fixation process; I have asked a colleague to use her brain sections. Using my staining protocol and same antibody I was able to view an amazing signal, located in the nucleus and with a really good signal to noise ratio.

There are some differences between out post-fixation protocols.
The protocol I use for post-fixation is:
96 hours in 0.01M PBS + 30% sucrose + 1% PFA in 4C.
after the brain has sinked I take it out and freeze the brain in -80C
couple of days \\ weeks later - I defreeze it and use the microtom to slice it.

Her post fixation is different than mine. First she keeps the brain in 0.01M PBS + 4% PFA over night, following by a gradient of PBS + sucrose (10% for 24 hours and then 20% for 24 more hours). She does not freeze the brain after the post fixation process, but keeps it in 4C until slicing.


What do you think causes my problem? Which protocol do you use?

Thanks in advance!
Karen.

#2 bob1

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Posted 02 February 2012 - 01:00 PM

The noise you are seeing is likely to be paraformaldehyde crystal residue in the tissue, I would switch to a PFA free post-fix. The gradient sucrose is probably more gentle on the tissue than going straight to 30%. At this point, freezing probably won't make much difference, though the thawing process might disrupt the cells a bit dur to ice crystal formation.

#3 scolix

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Posted 03 February 2012 - 12:40 PM

Don't use PFA during dehydration, just use 30% sucrose.





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