Examples of 'assessed by flow cytometry' in a sentence
Meaning of "assessed by flow cytometry"
assessed by flow cytometry - This phrase indicates that a particular assessment or evaluation process is being conducted by using flow cytometry, which is a technique for counting, examining, and sorting microscopic particles suspended in a stream of fluid. It is commonly used in various scientific and medical fields to analyze cells, biomolecules, and more
How to use "assessed by flow cytometry" in a sentence
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assessed by flow cytometry
The extent of reprogramming was assessed by flow cytometry.
Binding was assessed by flow cytometry using a FACScalibur flow cytometer.
The purity of the cells was assessed by flow cytometry.
Binding was assessed by flow cytometry using a BD FACSArray.
Expression of the adhesion protein is assessed by flow cytometry.
Neutrophil viability was assessed by flow cytometry using apoptotic and necrotic markers.
The binding of SIRPaFc fusión proteins to human erythrocytes was therefore assessed by flow cytometry.
Circulating EPCs were assessed by flow cytometry and cell culture.
After 24 hours the percentage of proliferating cells was assessed by flow cytometry.
Binding was assessed by flow cytometry.
Cells were harvested and GFP fluorescence assessed by flow cytometry.
The number of T cells is assessed by flow cytometry using counting beads as reference.
Following this incubation, expression of the reporter gene was assessed by flow cytometry.
Cell death was assessed by flow cytometry based on Annexin V staining.
Induction of T regulatory cells was assessed by flow cytometry.
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Apoptosis was simultaneously assessed by flow cytometry analysis of cells displaying annexin-V-positive staining.
Phosphorylation level of Stat5 was assessed by flow cytometry.
Cell death was assessed by flow cytometry analysis of AV and / or PI staining.
Induction of CRTH2 expression was assessed by flow cytometry.
Differential cell counts were assessed by flow cytometry ( LSRII ® cytometer, BD Bioscience ).
In these experiments MCF-7 tumor cells were treated with DC and assessed by flow cytometry.
Proliferation was assessed by flow cytometry.
Saccharomyces cerevisiae y440 mat a, leu2 cells had their growth and cell viability assessed by flow cytometry.
GFP expression was assessed by flow cytometry.
Purity of enriched monocyte fraction exceeded 90 % as assessed by flow cytometry.
NKG2D expression was assessed by flow cytometry at 48hr FIG.
The percent of cells expressing active capase-3 was assessed by flow cytometry.
YH2AX levels were assessed by flow cytometry.
Twenty-four hours after transfection, GFP-expression was assessed by flow cytometry.
SIINFEKL specific immunity was assessed by flow cytometry ( pentamer analysis ).
GFP expression, as a marker of NFAT activation, was assessed by flow cytometry.
DNA fragmentation may be assessed by flow cytometry.
Furthermore, the expression of PDGFRa and CD44 on TECs was assessed by flow cytometry.
Expression of M1 and M2 macrophage markers assessed by flow cytometry is shown in Figure 5b.
After 48hrs, cells were washed and NKG2D surface expression was assessed by flow cytometry.
Activation of caspase-3 was then assessed by flow cytometry.
Five days after adoptive transfer, the TCRMOG CD4 + T cells were assessed by flow cytometry.
DNA ploidy and S-phase fraction (SPF) was assessed by flow cytometry.
The percentage of CD4/CD25 double positive Tregs was assessed by flow cytometry.
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