Not exact matches
To determine the effect of the conditioned medium on NGF - induced neurite outgrowth, PC12 cells were dissociated and plated on polyornithine - coated tissue
culture dishes in the
following conditions: 1) HT22 conditioned medium, 2) J147 treated HT22 conditioned medium, 3) DMEM alone plus J147, 4) DMEM plus NGF at 50 nanograms per ml, 5) J147 treated HT22 conditioned medium pre-incubated for one hour with 10 μg / ml anti-NGF and N2 supplement (Invitrogen).
The colonies were fixed in
culture dishes with 4 % paraformaldehyde in phosphate - buffered saline (0.01 M PBS, pH 7.4) for 20 min at room temperature (RT)
followed by washing with PBS (2 × 5 min).
Human fetal NSCs (ReNCell VM, Chemicon) were
cultured on laminin - coated
dishes in ReNcell maintenance medium (Chemicon) in the presence of basic fibroblast growth factor 2 (bFGF2),
following the manufacturer's instructions.
Neuronal outgrowths in 24 - well tissue
culture dishes were fixed, permeabilized and blocked as above prior to staining with anti-β-III tubulin, 1 ∶ 200 (Chemicon mab1637
followed by secondary labeling with AF488 goat anti-mouse IgG1 (A21121, Invitrogen).