Fig. 4.
Fig. 4. Analysis by flow cytometry of Ficoll-Hypaque–purified leukapheresis products. Enumeration of CD34+ cells in light density cell suspension of peripheral blood labeled with anti-E2/NS1 whose labeling to the cells was defined by goat antimouse Ig conjugated with FITC. Surface (A) and cytoplasmic (B) stainings were performed. In (C), FITC-labeled isotypic control is shown. Double-staining analysis with PE-conjugated anti-CD34 antibody followed by FITC-labeled anti-E2/NS1 antibody is reported in (D). Isotypic controls are indicated in (E and F).

Analysis by flow cytometry of Ficoll-Hypaque–purified leukapheresis products. Enumeration of CD34+ cells in light density cell suspension of peripheral blood labeled with anti-E2/NS1 whose labeling to the cells was defined by goat antimouse Ig conjugated with FITC. Surface (A) and cytoplasmic (B) stainings were performed. In (C), FITC-labeled isotypic control is shown. Double-staining analysis with PE-conjugated anti-CD34 antibody followed by FITC-labeled anti-E2/NS1 antibody is reported in (D). Isotypic controls are indicated in (E and F).

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