Fig. 1.
Fig. 1. Combined DIC and fluorescence image (A), DIC image (B), and fluorescence images (A′, B′) of living neutrophils. / Cells were labeled at 4°C with anti-CD43 mAbs (A, A′) or anti-CD11b mAbs (B, B′) and TRITC-conjugated F(ab′)2 fragments of secondary antibodies. They were analyzed at 37°C as described in “Materials and methods”. (A, A′) Polarized, locomoting neutrophils with CD43 caps located at the uropods. (B, B′) Round, stationary neutrophils with uniformly patched CD11b. Scale bar = 10 μm. (Panel A, the top left corner cell is round, nonpolarized, and nonmotile.)

Combined DIC and fluorescence image (A), DIC image (B), and fluorescence images (A′, B′) of living neutrophils.

Cells were labeled at 4°C with anti-CD43 mAbs (A, A′) or anti-CD11b mAbs (B, B′) and TRITC-conjugated F(ab′)2 fragments of secondary antibodies. They were analyzed at 37°C as described in “Materials and methods”. (A, A′) Polarized, locomoting neutrophils with CD43 caps located at the uropods. (B, B′) Round, stationary neutrophils with uniformly patched CD11b. Scale bar = 10 μm. (Panel A, the top left corner cell is round, nonpolarized, and nonmotile.)

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