Figure 5
Figure 5. Isolation of tonsillar B-cell subsets based on CD77/CD10/IgD staining. Purified tonsillar B cells were triple-stained with FITC-conjugated anti-CD77, PE-Cy5–conjugated anti-CD10, and PE-conjugated anti-IgD mAbs to identify CD77+ centroblasts, and from the CD77− fraction, CD10+IgD− centrocytes, CD10−IgD+ non-GC cells (predominantly naive B cells), and CD10−IgD− non-GC cells (predominantly memory B cells) and then separated using the indicated sort gates. Isolated B-cell subsets were subsequently reanalyzed to determine the sort purities. Shown are representative data from donor CCT13.

Isolation of tonsillar B-cell subsets based on CD77/CD10/IgD staining. Purified tonsillar B cells were triple-stained with FITC-conjugated anti-CD77, PE-Cy5–conjugated anti-CD10, and PE-conjugated anti-IgD mAbs to identify CD77+ centroblasts, and from the CD77 fraction, CD10+IgD centrocytes, CD10IgD+ non-GC cells (predominantly naive B cells), and CD10IgD non-GC cells (predominantly memory B cells) and then separated using the indicated sort gates. Isolated B-cell subsets were subsequently reanalyzed to determine the sort purities. Shown are representative data from donor CCT13.

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