Diluted AF488-2B1 binds specifically with polystyrene beads. The overlaid plots are obtained from five interday analyses (see Supporting S2 Table, online). There were no significant differences among the five scatter plots, as tested by analysis of covariance (ANCOVA) (p = 0.9208).</p
Several methods have been proposed for comparing fluorescence intensity curves obtained from flow cy...
Affinity panning of large libraries is a powerful tool to identify protein binders. However, panning...
Selection of cells labeled with fluorescein isothiocyanate-conjugated (FITC) antibodies can be diffi...
The fluorescence detected using fluorochrome-labelled monoclonal antibodies depends not only on the ...
adhesion molecules(PECAM-1), is expressed on the surface of endothelial cells, platelets, monocytes/...
Flow cytometry is an established method for fast and ac-curate quantitation of cellular protein leve...
The use of antibodies in immunodiagnostic kits generally implies the conjugation of these proteins w...
<p>Schematic illustration of scaling effect on particle-antibody complexes (upper figure). Relations...
The interrogation of single cells is revolutionizing biology, especially our understanding of the im...
<p>A, C: Neighbouring sections through a needle track 30 days after the lesion. In A, no primary ant...
A microfabricated flow cytometer has been developed for the analysis of micron-sized polymer beads o...
<p>A representative cytofluorometric analysis of a freshly isolated GD2 positive cell preparation, t...
Accurate measurement of antigen-positive cells by flow cytometry can be hampered by background fluor...
Within the scientific literature, analyses of data from bead based multiplex immunoassays are based ...
<p>(A) A mixture of CMFDA<sup>-</sup> and CMFDA<sup>+</sup> platelet MPs (CMFDA<sup>- and +</sup>) a...
Several methods have been proposed for comparing fluorescence intensity curves obtained from flow cy...
Affinity panning of large libraries is a powerful tool to identify protein binders. However, panning...
Selection of cells labeled with fluorescein isothiocyanate-conjugated (FITC) antibodies can be diffi...
The fluorescence detected using fluorochrome-labelled monoclonal antibodies depends not only on the ...
adhesion molecules(PECAM-1), is expressed on the surface of endothelial cells, platelets, monocytes/...
Flow cytometry is an established method for fast and ac-curate quantitation of cellular protein leve...
The use of antibodies in immunodiagnostic kits generally implies the conjugation of these proteins w...
<p>Schematic illustration of scaling effect on particle-antibody complexes (upper figure). Relations...
The interrogation of single cells is revolutionizing biology, especially our understanding of the im...
<p>A, C: Neighbouring sections through a needle track 30 days after the lesion. In A, no primary ant...
A microfabricated flow cytometer has been developed for the analysis of micron-sized polymer beads o...
<p>A representative cytofluorometric analysis of a freshly isolated GD2 positive cell preparation, t...
Accurate measurement of antigen-positive cells by flow cytometry can be hampered by background fluor...
Within the scientific literature, analyses of data from bead based multiplex immunoassays are based ...
<p>(A) A mixture of CMFDA<sup>-</sup> and CMFDA<sup>+</sup> platelet MPs (CMFDA<sup>- and +</sup>) a...
Several methods have been proposed for comparing fluorescence intensity curves obtained from flow cy...
Affinity panning of large libraries is a powerful tool to identify protein binders. However, panning...
Selection of cells labeled with fluorescein isothiocyanate-conjugated (FITC) antibodies can be diffi...