[Histonet] mouse heart morphology
David McClister
mcclistd <@t> musc.edu
Mon Mar 7 12:29:42 CST 2005
Here is some more info about my situation with these mice hearts. Once the heart is extracted, it is put in saline 5 min, blotted dry, longitudinally cut and frozen in a mixture of ethanol and dry ice then stored in -80. The temperature of the crystat is -20. When the heart is cut, I cannot see the RV and LV chambers just one big heart. I'm doing a H&E and taking a 1x image to see the heart. Dentamold has been used in the past to keep the chambers separate but I could not get quality sections cutting through it. Does anyone have any suggestions how I can make the morphology
of frozen tissue comparable to paraffin embedded tissue?
Thanks again,
Dave McClister
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