Dear Histonetters,

First of all Merry Christmas and Happy New Year to all!! I have a question
that hopefully someone will have an answer.

We have grown up some cells in a petri dish. We are now wanting to try and
process these cells, however, we need to keep them in their shape and not
disrupt them. Does anyone have an idea of how to do this or reference to
journal articles that would contain this information?

I thought we could place the cells in agar and then process them but don't
know what type of agar would process and cut well. Would like any imput
possible.

Also, is there anyone out there that knows of a cytology network like our
histonet?

Thanks for your help everyone! Happy Holidays!

Sincerely,
Lynn Gardner