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. 2008 Dec 12;1:2. doi: 10.3389/neuro.16.002.2008

Figure 2.

Figure 2

Micropatterned coverslip preparation scheme. (A) A polyethyleneimine (PEI)-coated coverslip was placed on top the PDMS mold with the PEI-coated side facing the PDMS mold as shown in (B). (C) Boiling agarose (2% w/v in water) was added to one of the open ends while gentle suction was applied at the other end to draw agarose into the channel until it was completely filled. The agarose was allowed to cool down and then the micropatterned coverslip was removed from the PDMS mold. (D) The micropatterned coverslip consists of a micropit array in the middle portion with non-pit segmental regions on each side. Plating and culturing astrocytes on these micropatterned coverslips yields cells grown in the micropit regions as shown in the schematic diagram in (E) as well as grouped cells in the two non-micropit regions on either side.