<p>We used the flow cytometry to detected the phenotype of CTLs. (A) control CTLs without labeled; (B) CTL were stained with monoclonal antibodies specific for CD3 (FITC labeled) and CD8 (PE labeled); (C) CTL were stained with monoclonal antibodies specific for CD3 (FITC labeled) and CD56 (PE labeled); (D) CTL were stained with monoclonal antibodies specific for CD226 (FITC labeled) and CD11a (PE labeled); (E) CTL were stained with monoclonal antibodies specific for CD305 (FITC labeled) and CD11a (PE labeled).</p
<p>To determine the percentage of MDSCs in patients, fresh whole blood was incubated with a combined...
<p>Cells were isolated from NSCLC patient samples using an antibody against MUC1. (A) Cells were the...
<p>A cocktail of antibodies with 8 fluorochromes was used to label PBMC with anti-CD8, lineage marke...
The purpose of this study was to optimize a fixation procedure for detection of cytoplasmic antigens...
<p>(A) Flow cytometry analysis for MSCs. The red open histograms indicated the cells which were stai...
<p>As described above we detected a variety of CTC subtypes. N-cadherin and CD133 were stained on se...
(A) CTSL was measured in different tissue cells by sandwich ELISA. Values represented as mean ± SEM ...
<p>After exclusion of debris (A) and selection of CD45− (B), nucleated (Syto16+) and CD31+ cells (C)...
<p>(A) Phenotypic changes in expression of CD40, CD80 and CD86 maturation markers in TCL-loaded DCs ...
<p>Cells were stained (A) with fluorescently labelled antibodies against cell surface Fcγ receptors ...
MSCs were phenotypically characterized by flow cytometry using the stem cell markers CD73, CD90 and ...
<p>MSCs were harvested and analysed with flow cytometry for a panel of MSC-characterizing markers on...
<p>(A) Profiles of representative TIL cultures (specimen M27, TIL cultures 2 and 8) stained for CD3,...
<p>For CTC enumeration, EpCAM-positive cells were first isolated from patient blood samples, after w...
The development of flow cytometric biomarkers in human studies and clinical trials has been slowed b...
<p>To determine the percentage of MDSCs in patients, fresh whole blood was incubated with a combined...
<p>Cells were isolated from NSCLC patient samples using an antibody against MUC1. (A) Cells were the...
<p>A cocktail of antibodies with 8 fluorochromes was used to label PBMC with anti-CD8, lineage marke...
The purpose of this study was to optimize a fixation procedure for detection of cytoplasmic antigens...
<p>(A) Flow cytometry analysis for MSCs. The red open histograms indicated the cells which were stai...
<p>As described above we detected a variety of CTC subtypes. N-cadherin and CD133 were stained on se...
(A) CTSL was measured in different tissue cells by sandwich ELISA. Values represented as mean ± SEM ...
<p>After exclusion of debris (A) and selection of CD45− (B), nucleated (Syto16+) and CD31+ cells (C)...
<p>(A) Phenotypic changes in expression of CD40, CD80 and CD86 maturation markers in TCL-loaded DCs ...
<p>Cells were stained (A) with fluorescently labelled antibodies against cell surface Fcγ receptors ...
MSCs were phenotypically characterized by flow cytometry using the stem cell markers CD73, CD90 and ...
<p>MSCs were harvested and analysed with flow cytometry for a panel of MSC-characterizing markers on...
<p>(A) Profiles of representative TIL cultures (specimen M27, TIL cultures 2 and 8) stained for CD3,...
<p>For CTC enumeration, EpCAM-positive cells were first isolated from patient blood samples, after w...
The development of flow cytometric biomarkers in human studies and clinical trials has been slowed b...
<p>To determine the percentage of MDSCs in patients, fresh whole blood was incubated with a combined...
<p>Cells were isolated from NSCLC patient samples using an antibody against MUC1. (A) Cells were the...
<p>A cocktail of antibodies with 8 fluorochromes was used to label PBMC with anti-CD8, lineage marke...