In this study, Nicchitta and his colleagues
treated tissue culture cells with a stress - inducing agent called thapsigargin.
Not exact matches
At the time, his varied interests — in the use of skin
cell culture to
treat burns, in human
tissue cultures, and in biopharmaceutical production — led him to do his final year, 6 - month project on
culture in a bioreactor.
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).
Briefly, NHLF
cells were grown in 96 - well CoStar
tissue culture plates (4,000
cells per well) and either subjected to siRNA gene silencing or directly
treated with compounds for 51hours in 100 µL complete medium per well.
Cells were then plated in 24 - well
tissue culture treated plates and incubated in a humidified 5 % CO2 incubator at 37 °C.
For induction of differentiation to mature endothelial
cells, EPCs were plated at a high
cell density (8 × 104
cells / cm2) on
tissue culture treated flasks.
HEK293T
cells were seeded at 2 × 107
cells in 15 - cm
tissue culture plates and
cells were
treated with 20 mM LiCl for 7 hr.