Examples of 'flow cytometric analysis' in a sentence
Meaning of "flow cytometric analysis"
Flow cytometric analysis is a technique used in biology and medicine to study and analyze cells and other particles in a fluid suspension. It involves passing cells through a laser beam and measuring the light scatter and fluorescence emitted by the cells
How to use "flow cytometric analysis" in a sentence
Basic
Advanced
flow cytometric analysis
Flow cytometric analysis has been described above.
Bound protein was detected using flow cytometric analysis.
Flow cytometric analysis of cell cycle distribution.
Transfected cells were also examined by flow cytometric analysis.
Flow cytometric analysis of lymphocyte markers.
Expression of eGFP protein was analysed by flow cytometric analysis.
Flow cytometric analysis of cell surface activation markers.
Cytokine production was detected by flow cytometric analysis as previously described.
Flow cytometric analysis of mesenchymal stem cell surface molecules.
Toxicity was assessed by flow cytometric analysis of cellular light scatter.
Flow cytometric analysis of samples prepared for the sorting experiment.
Toxicity can be assessed by flow cytometric analysis of cellular light scatter.
Flow cytometric analysis of antibody binding to human peripheral blood cells.
Samples were also collected for flow cytometric analysis as described herein.
Standard flow cytometric analysis assessed surface expression of various markers.
See also
The thus obtained cell suspension was used in a flow cytometric analysis.
B cell flow cytometric analysis.
The cells are counted and phenotypically characterized by flow cytometric analysis.
According to flow cytometric analysis the latter line was diploid.
The cells were then subjected to staining and flow cytometric analysis.
This has been demonstrated by flow cytometric analysis using indirect immunofluorescence.
Aliquots of the marrow were stained with antibodies for flow cytometric analysis.
Unstained flow cytometric analysis of both cell preparations were performed as described above.
The purity of sorted cells was confirmed by flow cytometric analysis immediately after sorting.
Flow cytometric analysis is performed on a FACSCalibur instrument and analyzed with CellQuest software.
The procedure for single color flow cytometric analysis has been previously published.
The cell surface expression of either receptor was analyzed using flow cytometric analysis.
Flow cytometric analysis showed that morroniside and loganin inhibited the cell cycle of rat MCs.
Single cell suspensions were then used to measure EdU incorporation flow cytometric analysis.
Flow cytometric analysis of stained Jurkat cells.
Infections were detected by immunofluorescence staining followed by either microscopy or quantitative flow cytometric analysis.
Dendritic cell phenotype and morphology were confirmed by flow cytometric analysis and scanning electron microscopy.
Flow cytometric analysis is to characterize the immunophenotype of ex vivo expanded DPSC.
Spleens and femurs were processed to obtain erythroid precursor cells for flow cytometric analysis.
Cultures for flow cytometric analysis of NK cell activation.
Each spleen was enumerated separately and then pooled together for flow cytometric analysis.
Proceed with flow cytometric analysis using Dako MoFlo.
Additionally preferred assays for analyzing the present polyspecific binding proteins involve flow cytometric analysis.
Proceed with flow cytometric analysis using Dako MoFIo.
The presence of TF was also confirmed by flow cytometric analysis.
Cell surface staining Flow cytometric analysis was carried out as follows.
Flow cytometry Cells were phenotyped using flow cytometric analysis.
Flow cytometric analysis At the time of sacrifice spleen weights were recorded.
The DNA content was determined by flow cytometric analysis.
Flow cytometric analysis was performed using a COULTER EPICS instrument.
Surface expression of the HA protein was determined using flow cytometric analysis.
The test results between MxA EIA and flow cytometric analysis showed significant correlation.
Propodium iodide stained cells were analysed for DNA content using flow cytometric analysis.
Flow Cytometric Analysis for the detection of donor derived cells.
The dispersed cells were then washed and resuspended in PBS for flow cytometric analysis.
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