Examples of 'cytometric analysis' in a sentence
Meaning of "cytometric analysis"
Cytometric analysis is a technique used in biological and medical research to study and analyze cells. It involves the measurement of various physical and chemical characteristics of cells, such as size, shape, and DNA content. This analysis is done using flow cytometry, a method that uses laser beams and detectors to collect and analyze data from individual cells or particles in a fluid stream
How to use "cytometric analysis" in a sentence
Basic
Advanced
cytometric analysis
Cytometric analysis of cell phenotype and function.
Bound protein was detected using flow cytometric analysis.
Flow cytometric analysis has been described above.
Data was analyzed using FlowJo cytometric analysis software.
Flow cytometric analysis of cell cycle distribution.
Transfected cells were also examined by flow cytometric analysis.
Cytometric analysis is conducted as described above.
Expression of eGFP protein was analysed by flow cytometric analysis.
Flow cytometric analysis of lymphocyte markers.
Cytokine production was detected by flow cytometric analysis as previously described.
Flow cytometric analysis of cell surface activation markers.
B cell flow cytometric analysis.
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.
See also
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.
The thus obtained cell suspension was used in a flow cytometric analysis.
According to flow cytometric analysis the latter line was diploid.
The cells are counted and phenotypically characterized by flow cytometric analysis.
This has been demonstrated by flow cytometric analysis using indirect immunofluorescence.
The cells were then subjected to staining and flow cytometric analysis.
Unstained flow cytometric analysis of both cell preparations were performed as described above.
Aliquots of the marrow were stained with antibodies for flow cytometric analysis.
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.
Kinetic cytometric analysis revealed a significant immune infiltrate during and prior to tumor regression.
The purity of sorted cells was confirmed by flow cytometric analysis immediately after sorting.
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 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.
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.
For the detection of dead cells propidium jodid was added immediately before cytometric analysis.
Proceed with flow cytometric analysis using Dako MoFIo.
Additionally preferred assays for analyzing the present polyspecific binding proteins involve flow cytometric analysis.
Cell surface staining Flow cytometric analysis was carried out as follows.
The presence of TF was also confirmed by flow cytometric analysis.
Flow cytometric analysis is to characterize the immunophenotype of ex vivo expanded DPSC.
The DNA content was determined by flow cytometric analysis.
Flow cytometric analysis At the time of sacrifice spleen weights were recorded.
Flow cytometry Cells were phenotyped using flow cytometric analysis.
Flow cytometric analysis was performed using a COULTER EPICS instrument.
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Cytometric analysis of cell phenotype and function
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