Primary cortical cultures
seanpat at FMED2.UNCU.EDU.AR
Fri Oct 8 08:02:29 EST 1999
> I am preparing primary cultures from E16-E18 mouse embryos. I would
>like to get single neuronal cells, however I end up with large
>aggregates with large neuritic outgrowths. This makes it difficult for
>single cell analysis. Any suggestions? Your attention to this matter
>would be appreciated greatly.
How are you disaggregating your cells? You may need to increase your enzyme
treatment or trituration procedures.
Sean Patterson, Ph.D.
Catedra de Fisiologia, CC33
Facultad de Ciencias Medicas
Universidad Nacional de Cuyo
Tel: (0261) 430-9385
Fax: (0261) 449-4117
e-mail: seanpat at fmed2.uncu.edu.ar
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