Sentence examples for markers using flow from inspiring English sources

The hippocampus was dissected 1 h after the second exposure, and DG neurons were examined for activation markers using flow cytometry.

Mice were sacrificed after 2 weeks, and splenocytes were stained for the expression of H2kb, H2kd, and immune cell lineage markers using flow cytometry18,19.

In this experimental study BM-MSCs were cultured and the cells characterized by analysis of cell surface markers using flow cytometry.

(A) Detection of less differentiated T cell markers using flow cytometry for T cells generated by OKT3/IL-2 (OKT3), OKT3-28BBZ RNA electroporation (OKT-28bb-1) OKT3-28BBZBBZ, CD86 and 4-1BBL RNA co-electroporation (OKT-28bb-2).

Recent advances in the identification of specific neural cell types based on cell surface and intracellular markers, using flow cytometry, have lead to detailed characterization of neural stem and progenitor cells, as well as their down-stream progeny.

One option would be to additionally assess amount and functional capacities of Tregs by additional markers using flow cytometry and functional suppression assays [4], [13], however this is generally not feasible in large field studies.

To characterize the composition of the LacZ+-positive cell population in the myocardium, we used Sca-1 and ckit (CD117) to identify progenitor populations, CD31 to detect endothelial cells; CD45 was used as a common leukocyte marker, using flow cytometry.

Peripheral white blood cells were analysed for the expression of endothelial progenitor cell characterizing surface markers by using flow cytometry as previously described [ 12].

Also, surface marker studies using flow cytometry showed a pattern similar to that known from normal hMSC.

The rate of cell proliferation was significantly increased due to presence of R-peptide, and the MSCs marker analyses using flow cytometry and immunocytochemistry staining proved the ability of R-peptide to maintain mesenchymal stem cell properties (high proliferation, expression of multipotent markers and differentiation capacity) even after long-term passage culturing.

More than 85% of the remaining adherent cells were TAMs, as assessed by macrophage-specific marker F4/80 using flow cytometry.