Examples of 'flow cytometry using' in a sentence
Meaning of "flow cytometry using"
flow cytometry using: This phrase indicates the method of applying flow cytometry, a technique used to analyze cells or particles in a fluid stream, for a specific purpose
How to use "flow cytometry using" in a sentence
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flow cytometry using
Samples were analyzed by flow cytometry using a FACSCaliber.
Enrichment was monitored using restriction fragment length polymorphism ( RFLP ) and flow cytometry using live cells.
Samples are analyzed by flow cytometry using standard techniques.
The distribution of the 2 different antibody specificities was determined by flow cytometry using fluorescently-labelled antigen.
The method includes flow cytometry using fluorescent antibody technique and the like.
Thereafter, the cells are analyzed by flow cytometry using FACScan.
Samples were analysed by flow cytometry using a FACScalibur and CellQuest software ( Becton Dickinson ).
In another instance, the enrichment is accomplished by flow cytometry using the fluorescent label.
Figure 21, Flow Cytometry using stained bone marrow cells.
The stained cells were resolved by flow cytometry using standard methods.
Binding was assessed by flow cytometry using a FACScalibur flow cytometer.
After washing in PBS / BSA, fluorescence may be measured by flow cytometry using standard methods.
Binding was determined by flow cytometry using an isotype control.
Cell cycle analysis was performed by flow cytometry using propidium iodide.
Measurements were obtained by flow cytometry using propidium iodide staining.
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The proportion of OX40L bound was then detected by flow cytometry using a labelled secondary reagent.
T cells are sorted by flow cytometry using the suggested markers above.
Cell viability and cell number were determined by Flow Cytometry using the Guava EasyCyte 6HT/2L.
Neutrophil viability was assessed by flow cytometry using apoptotic and necrotic markers.
HLA A2 expression on these cells was analyzed by flow cytometry using BB7.2 antibody.
The study was performed by flow cytometry using a FACScan to analyze the samples.
Stained cells were then detected by flow cytometry using standard methods.
Cell numbers were quantified by Flow Cytometry using the Guava EasyCyte and ViaCount Reagent.
Increased class II antigen expression is determined by flow cytometry using the appropriate secondary antibodies.
Binding was determined by flow cytometry using FITC-conjugated mycobacteria.
T lymphocyte characterization was done by flow cytometry using the following panels, act.
Cells were stained for analysis by flow cytometry using different fluorchrome-conjugated antibodies.
The cells were washed prior to analysis by flow cytometry using a FACScalibur ( Becton Dickinson ).
MAb binding was revealed by flow cytometry using PE-conjugated anti-rat IgG mAb.
The cells were analyzed by two-color flow cytometry using a Coulter Elite FCM.
Cell binding was analyzed by flow cytometry using ENG-expressing mouse B16 cell.
At day 6, BrdU incorporation was detected by flow cytometry using an anti-BrdU antibody.
Binding was assessed by flow cytometry using a BD FACSArray.
The binding was analyzed by flow cytometry using a BD FACSArray.
Cells were analyzed immediately by flow cytometry using a FACScanto II apparatus.
The number of T cells is assessed by flow cytometry using counting beads as reference.
The degree of staining was determined by flow cytometry using a Becton Dickinson FACScan flow cytometer.
The expression of MHC class I is detected by flow cytometry using a specific fluorescent labelled antibody.
Binding of the polypeptide is determined by flow cytometry using a Fluorescence Activated Cell Sorter.
The cells were analyzed by two-color flow cytometry using a Coulter Elite flow cytometer.
The cell culture viability was measured by flow cytometry using Fluorescence-Activated Cell Sorting.
Ten thousand events were analyzed immediately by flow cytometry using a MACSQuant Analyzer ( Miltenyi Biotec ).
Apoptotic and necrotic cells were followed by flow cytometry using an annexin-V-FITC/P1 kit.
The cell suspension is then examined by flow cytometry using a 488 nm argon laser for excitation.
The cells were then analysed by flow cytometry using a FACScan ( BD ).
The binding affinity was measured by flow cytometry using CAL-27 tumor cells.
Cell concentration was evaluated by flow cytometry using Perfect-Count Microsphere ™ ( Cytognos ).
The samples were generally run and analyzed by flow cytometry using FACSortR ( Becton & Dickinson ).
Cells were analyzed for expression by flow cytometry using antibodies specific for HLA-A and H-2Kb.
DCs survival was determined by flow cytometry using the 7-AAD assay.
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