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Then, sections were incubated for 60 min with various concentrations of [18F]exendin-4 (range 2.5 20 nM) in vitro.
The microparticles showed high swelling capacity within 5 min, with various sustained drug release rates depending on chitosan concentration and molecular weight.
In fact, stimulation of striatal cultures for 15 min with various concentrations of CRF up to and including 400 nM (Figure 3C) failed to induce a significant accumulation of cAMP.
Serial 3-fold dilutions of kinase inhibitors were injected for 1 min with various dissociation times.
LUVs with entrapped calcein in a suspension containing 2.5 μM lipid were then incubated for 25 min with various concentrations of peptide (0.03 0.25 μ).
Viable and fully mature stage V gametocytes were incubated for 15 min with various KAF156 concentrations and fed to mosquitoes through an SMFA.
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Breads with varying texture were prepared under various dough mixing conditions and formats, different baking times (8, 11, 15 and 17 min), and with various contents of bioprocessed fibres.
Cells were then incubated either with CytD (10µg/ml) for 30 min or with various chromophoric cytotoxic drugs (Table 1) for 24 hr at 37°C.
All the luminescent images were acquired after 4 min scanning with various filters.
Physical activity training consisted of two weekly 60-min sessions with various dynamic activities.
The kinetic parameters of TDIs 3′EF, 4′EF, 5EF, 6EF, and 7EF in the inhibition of P450 1A1 were determined through a 6 min continuous observation with various concentrations of the inhibitors.
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