Sentence examples for murine cells we from inspiring English sources
To determine the SASPs of murine cells, we collected serum-free conditioned media (CM) from PRE, SEN(OXI) and SEN XRA) cells, normalized for cell number, and analyzed the CM using antibody arrays designed to detect 62 proteins selected for roles in intercellular signaling.
For murine cells, we observed that only CXCL10 could significantly increase cell survival within 5 days of serum starvation.
Using publicly available microarray data from murine cells, we have shown that a pattern of differential prognosis emerges from assessment of similarity with known pathway signatures.
Examining sets of genes that were highly upregulated in murine cells, we found that many orthologous human genes were also significantly upregulated in t(8 21) AML patients.
To check the expression of mmu-miR-127 in the murine cells, we used the same primer set and Taqman probe (Cat 000452, Applied Biosystems, Applera) used for human cells, as the sequence homology was 100%.
To validate the results obtained in murine cells, we assessed the impact of p110δ inactivation in human T cell allorecognition in an adapted mixed lymphocyte reaction (MLR) assay using HCs from the blood of healthy donors in the presence of either LY or IC.
It had already been shown that human cells are much more susceptible to CGs than murine cells, as we also report here.
Since IFNγ can upregulate IRG expression in C. trachomatis infected murine cells [28], we investigated the involvement of IRGs in IFNγ-mediated inhibition of chlamydial growth.
It was hypothesized that STAT3 signaling would be elevated during myogenesis as it is essential for both proliferation and differentiation in murine cells, and we expected STAT1 phosphorylation to be restricted to proliferation.
This is likely due to a higher level of ecto-ATPase activity by murine cells since we observed that exogenous ATP added to murine macrophages rapidly became undetectable in contrast to the same amount of exogenous ATP added to human macrophages.
Using the microglial cell line, BV-2, as well as primary murine microglial cells, we show here that the β-adrenergic agonist, isoproterenol, suppresses uptake of hydrophobic polystyrene microspheres.
