Hi Joel, 

Lipids are fixed only by OsO4, so you need to use it as a post-fixative.
As a fixative in our lab we use Karnovsky fixative, then we use osmium 
tetroxide as a post-fixative/fixative for the lipids for 15 min. Then we wash 
in Na-cacodylate buffer for 5 min, and then dehydrate, starting with two 
changes of 70% ethanol ( for 10min.) and then we go to two changes of 95% and 
then absolute ethanol, followed by two changes of abs. acetone, then 50:50 
acetone:resin and 2 changes of resin, then embedding and polymerization at the 
right temperature.

If your lipids are fixed properly they will be round droplets with 
characteristic appearance. OsO4 will blacken the tissue.
We always have excellent results with this protocol.

Hope that was helpful,

Iliana dimitrova,
Memorial university of Newfoundland,
Canada

-----Original Message-----
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Joel Haas
Sent: June-05-13 3:00 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Electron Microscopy protocols

Hello all,
    I am working on developing an electron microscopy protocol for looking at 
lipid droplets in cultured cells. We have used thin section TEM previously and 
found that the morphology of the droplets is often deformed (should be 
spherical, shows up as egg shaped or lumpy). If possible we would like to avoid 
these types of preservation artifacts. Does anyone have suggestions for 
adapting the protocol to better preserve these types of structures--a 
triglyceride lipid core surrounded by a phospholipid monolayer?

Thanks in advance,
Joel
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