Hello,
We have an ongoing debate in our lab regarding the relative virtue of heat
drying slides vs RT air drying them.
Tissues: 4% paraformaldehyde perfused rat brains frozen in OCT blocks
Sections: 10 microns on a cryostat (at approx -25 C)
Slides: Superfrost Plus
The slides are stored in slide boxes at -80 C until staining.
When staining the heat dry faction (wanting to avoid icy slides) put their
slide boxes straight out of the freezeer into a 50 C oven for 30 minutes before
taking out slides to stain. then the box goes back to the freezer until the
next round of staining,
The air dry group feels that cooking the antigens repeatedly at 50 C is
problematic so they take the frosty slides out their slide boxes and return
them ASAP to the freezer. The slides to be stained are air dried in the fume
hood for about 30 min.
A third, middle of the road, person takes her slides out of the cold boxes and
then puts the slides in a 60 C oven for 30 minutes.
For all three groups then, the slides are given a PAP pen border to prepare for
IHC and when the pen solution is dry, 10 minutes in acetone and the remainder
of the staining procedure.
So my question is: Who is using the best technique?
Another hotly debated topic is wether it is advisable to put a drop of PBS on
the slide before 'sticking' the section to prevent folds in the sections..
Any opinions are appreciated.
Thanks,
Jeff
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