Sentence examples for neurons were seeded from inspiring English sources

For neuronal viability assays, neurons were seeded in 24-well plates at a density of 20,000 30,000 cells per well or in 12-well plates at 80,000 100,000 cells per well and allowed to mature 6 7 days.

To study the cytocompatibility and cell behavior on the SF/TSF nanofibers, MSCs, VECs, and Neurons were seeded onto the nanofibers.

For transfection, E16.5 mouse post-mitotic neurons were seeded in 12-well plates at about 3 × 10^5 cells/well in 600 μl Neurobasal A-based differentiative medium.

To address this question, the hippocampal neurons were seeded on the polydimethylsiloxane (PDMS) substrate with different stiffness, which were coated with fibronectin and laminin respectively.

When primary neurons were seeded into the hydrogel, a massive array of three-dimensional (3D) neuron cultures were established with each of the cylinders containing a distinct gradient profile.

Briefly, following electroporation (Amaxa Nucleofector II), neurons were seeded onto poly-D-lysine coated coverslips in 12-well plates.

Neurons were seed at a density of 5 × 10 cells per well on round glass coverslips and, incubated under culture conditions of 37°C and 5 %CO2.

When primary cortical neurons (Cx) were cultured at high density in the left chamber of the device and hippocampal neurons (Hi) were seeded at low density in the right chamber, cortical neurons projected axons through the funnel-shaped micro-channels and established synapses with hippocampal neurons in the right chamber.

For immunostaining of single cultured hippocampal neurons, cells were seeded at a density of ~65 cells/mm on 13-mm poly-L-Lysine-coated coverslips placed in 24-well plates and cultured for 21 days in vitro (DIV).

In case of primary spinal neurons, dissociated tissues were seeded onto a poly-D-lysine-coated cover slip and incubated for 14 days (DIV14) under appropriate conditions (see above).

For neurons cortical isolates were seeded at a density of 1.2×105 cells/well on poly-D-lysine coated cover slips, placed in 24-well plates and maintained for 10 days in neurobasal medium supplemented with 2% B27 (Invitrogen), penicillin/streptomycin and 0.5 mM L-glutamine (Invitrogen).