[Histonet] brain embedding
I was wondering if anyone has familiarity with embedding fixed rat brain tissue using agar or agarose for sectioning on a vibrating microtome (Vibratome)? My supervisor feels that it might be worthwhile to consider embedding our tissue using these procedures since it might facilitate sectioning on a vibratome. (We often want to collect sections that could potentially range from 20 to 40 microns depending on experimental procedure). Would someone be able to provide me with a detail procedure and/or protocol for embedding rat brain tissue? Also is there a reason for why one should use agar versus agarose for embedding? And could this embedding procedure potentially interfere with immunostaining?
I appreciate your help and any suggestions,
Histonet mailing list
<< Previous Message | Next Message >>