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Culturing treated polyps both under normal feeding and starvation regimes revealed an intense accumulation of fluorescent particles within the subhypostomal region, often shaping a ring like structure, more pronounced in starved animals (Figure 8).
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These cells were routinely cultured in 100 mm tissue culture treated polystyrene (TCPS) dishes.
The cells were cultured in 75 cm tissue culture treated flasks at 5% CO2 and 37 °C.
However, methanogenic activity was observed in cultures treated with alkali.
Glioblastoma cell photoinactivation was observed in cell cultures treated with ZnPc as well as with TAZnPc.
In further examinations, the mean viable bacterial counts in cultures treated with aztreonam-cefozopran were 1log lower than those in cultures treated with cefozopran alone.
Cultures were treated with 1 µM -JQ1 concurrent with the switch to DM. Cultures treated with -JQ1, DMSO, or left untreated (DM only) served as negative controls.
Cells were seeded in recommended growth media in black 384-well tissue culture treated plates at 500 cells per well.
(c) Flow cytometry of EYFP-positive cells from iNGN (iPSC) cultures treated with TAT-Cre over subsequent passages (P).
Lactic acid was observed in controls (720 mg L−1) and cultures treated with alkali (600 mg L−1).
Morphologic deterioration of Anaplasma, as determined by LM and EM, occurred in cultures treated with the same drug concentrations.
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