Figure 1
Figure 1. CD56+ cells from human peripheral blood harbor CD14+ cells, which resemble intermediate-sized lymphocytes. CD56+ cells were isolated from PBMCs using CD56 microbeads and magnetic-activated cell sorting technology. Purified CD56+ cells were stained for CD56 or CD14 and analyzed with a flow cytometer. (A-B) Step-wise arbitrary gating of subsets with increasing FSC identified a CD14+ cell population with scatter properties characteristic of intermediate-sized lymphocytes. (C) Plotting of CD14 expression against FSC resulted in the segregation of the CD14+ population from the lymphocytes. (A,C) Backgating of CD14+ cells (C) in the multicolor mode visualized the CD14+ population in the FSC/SSC histogram within the lymphocyte population (A gray dots). Results shown are from 1 representative donor (n = 21).

CD56+ cells from human peripheral blood harbor CD14+ cells, which resemble intermediate-sized lymphocytes. CD56+ cells were isolated from PBMCs using CD56 microbeads and magnetic-activated cell sorting technology. Purified CD56+ cells were stained for CD56 or CD14 and analyzed with a flow cytometer. (A-B) Step-wise arbitrary gating of subsets with increasing FSC identified a CD14+ cell population with scatter properties characteristic of intermediate-sized lymphocytes. (C) Plotting of CD14 expression against FSC resulted in the segregation of the CD14+ population from the lymphocytes. (A,C) Backgating of CD14+ cells (C) in the multicolor mode visualized the CD14+ population in the FSC/SSC histogram within the lymphocyte population (A gray dots). Results shown are from 1 representative donor (n = 21).

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