Sentence examples for media and cellular from inspiring English sources

Treatment with Acanthopanax senticosides B prior to H2O2 (100 μM) exposure can increase cell viability significantly, lessen H2O2-induced cardiomyocyte morphological change, and inhibit augmentation of LDH activity in culture media and cellular MDA content markedly.

Culture media and cellular extracts were collected after 24 hours of normoxic or hypoxic conditions.

For transfection of 80 cm2 flasks the protocol was scaled up to 9 ml of media and cellular density to 6×105 proportional to the increased surface of adherence and optimised to have more than 70% confluence after 24 h in culture.

Conditioned media and cellular extracts from PC-3 cells, with and without INPP4B induction, were analyzed for several secreted and intracellular proteases.

The temporal profile of the system is governed by the set of ODE based on the model network that distinguishes media and cellular domains.

In vitro characteristics of liposomes (e.g., stability in various biological media, mucoadhesiveness and cellular uptake profiles) were evaluated along with the pharmacokinetic studies in rats.

Furthermore, TSP1 protein levels were also evaluated in chondrocyte conditioned media (secretome) and cellular extracts (proteome) by western blot analyses and in cartilage explant culture by immunohistochemistry.

The disappearance of labeled fatty acids from the media) and the cellular uptake) were similar during the incubation period (P > 0.05).

On the following day, cells were treated with erlotinib for 1 day and then protein levels of osteolytic factors (parathyroid hormone-related protein (PTHrP), IL-1β, 6, 8, 10, 11, GM-CSF, TNF-α and vascular endothelial growth factor (VEGF)) [ 19– 21] in the culture media and the cellular DNA contents were determined by immunoassays and a double-strand DNA Quantification Kit (Invitrogen).

After incubation, media were aspirated, and cellular RNA and protein were isolated.

The change in CypHer5E fluorescence, which is pH sensitive with minimal extra-cellular fluorescence in standard culture media and maximal intra-cellular fluorescence in acidic intra-cellular compartments such as the endosome, is used to monitor the effect of antibodies on internalization of the surface-expressed CAIX.