Incubating cultured cells with RK - 33 had a similar effect, knocking down DDX3 expression in cells that highly express this protein and hampering their ability to multiply.
Not exact matches
Animal
cells are
cultured from stem
cells and
incubated in a «bioreactor» into tissue that can be «harvested» and formed into familiar foods like meatballs, patties, and fish sticks.
The team pumped around 50 million rat liver
cells into each of five bare scaffolds, then
incubated the organs in
culture for two weeks.
The research builds on the team's previous work with a technique called three - dimensional
culture, which involves
incubating stem
cells in a floating ball - shaped aggregate, unlike traditional
cell culture in which
cells grow in a flat layer on the surface of a
culture dish.
The group reported growing multiple parthenogenetic embryonic stem
cell lines by
incubating eggs in a warm, low - oxygen
culture medium.
Specifically,
cell cultures from bone tissue were
incubated in 10 % DMEM containing 10 ng / ml TNF - α and 10 μg / ml fluorescent probe of acetylated LDL, DiI - Ac - LDL (Biochemical Technologies, Cambridge, MA), for 4 h.
Cells were harvested in the manner described above with the exception that during this labeling period, the rat anti-E-selectin mAb (10E9.6) conjugated to FITC replaced PE - conjugated 10E9.6.
Cells (5 × 104) were seeded in 12.5 cm2
culture flask and
incubated for 24 h to allow for
cell attachment and recovery.
Cells were then plated in 24 - well tissue
culture treated plates and
incubated in a humidified 5 % CO2 incubator at 37 °C.
For adenoviral transduction, HB1.F3
cells were
incubated with purified adenovirus (1 ∶ 1000 dilution in DMEM) for 4 h and then
cultured overnight in DMEM.
Therefore, twelve day old, DMSO - differentiated, Ara - C treated P19
cultures were
incubated with the proteasome inhibitors MG - 132 and lactacystin for four hours; this was sufficient to rescue Oct4 protein expression (Figure 1D), suggesting that these
cells do indeed synthesize new Oct4 protein.
After growing to a 60 % to 70 % confluence level,
cells were arrested with 1 ml of Colcemid solution (10 µg / ml)(Invitrogen) for every 50 ml
cell culture and
incubated at 37 °C for 2 hours.
The researchers took the leaf extracts by taking several
cell cultures and
incubated each of them with various concentrations of stinging nettle preparations, whilst adding TNF to stimulate inflammation.