Authors
Noel Derecki, James Cronk, and Jonathan Kipnis
Summary
Here, we describe a protocol in which single cells are isolated acutely from adult mouse brains, made into single cell suspensions, depleted of myelin debris, then stained for markers to determine microglial contents. Cells are fixed and read on a multicolor flow cytometer.Further details
The protocol was published on Protocol Exchange on 17 May 2012. To see the entire protocol, click on the source link.Advertisement
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