Figure 1.
Figure 1. Expression of adhesion receptors other than CD99 is not affected by CD99 gene inactivation. (A) Detergent lysates of bone marrow–derived neutrophils or complete lungs from WT (+/+), heterozygous (+/−), or homozygous (−/−) CD99 gene–inactivated mice were immunoblotted for CD99 or α-tubulin (as indicated). Band intensities normalized to α-tubulin control are indicated below the blots. (B) Endothelial cells isolated from skins of either WT mice or CD99−/− mice were immunoblotted for the indicated antigens; quantification of the signals was standardized to α-tubulin signals (indicated below). (C) Fluorescence-activated cell sorting analysis of bone marrow–derived polymorphonuclear neutrophils (PMNs) of CD99−/− (red) and WT mice (blue) for the indicated antigens; purple solid lines and light green dotted lines mark antibody-isotype controls for WT and CD99−/− mice, respectively. VE-cad, VE-cadherin.

Expression of adhesion receptors other than CD99 is not affected by CD99 gene inactivation. (A) Detergent lysates of bone marrow–derived neutrophils or complete lungs from WT (+/+), heterozygous (+/−), or homozygous (−/−) CD99 gene–inactivated mice were immunoblotted for CD99 or α-tubulin (as indicated). Band intensities normalized to α-tubulin control are indicated below the blots. (B) Endothelial cells isolated from skins of either WT mice or CD99−/− mice were immunoblotted for the indicated antigens; quantification of the signals was standardized to α-tubulin signals (indicated below). (C) Fluorescence-activated cell sorting analysis of bone marrow–derived polymorphonuclear neutrophils (PMNs) of CD99−/− (red) and WT mice (blue) for the indicated antigens; purple solid lines and light green dotted lines mark antibody-isotype controls for WT and CD99−/− mice, respectively. VE-cad, VE-cadherin.

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