Hello Everyone !

I isolated mixed cells from neonatal mouse cortices , and they are always contaminated with other cells (by imaging it appears that my astrocytes are even the least common population) .. any ideas what I can do to prevent this ?

I plate on pdl coated flasks , and shake the mixed cells when confluent (1 hr on 180 rpm to remove microglia) and (4-6 hrs on 250 rpm to remove opcs)

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