Fig. 3.
Fig. 3. Phenotypic analysis of CD4+CD8+ thymocytes from H-2b H-Y and H-2b 2C mice with the CD2 null mutation. Thymocytes from H-2b H-Y or H-2b 2C mice with or without the CD2 null mutation were stained with PE-labeled anti-CD4, FITC-labeled anti-CD8, and biotinylated MoAb to the indicated marker followed by Streptavidin Tricolor and analyzed in the FACScan flow cytometer. A total of 30,000 events were collected. The fluorescence level of the indicated molecule on gated CD4+CD8+ thymocytes with (dotted line) and without (solid line) the β2-microglobulin null mutation (β2mo) is shown.

Phenotypic analysis of CD4+CD8+ thymocytes from H-2b H-Y and H-2b 2C mice with the CD2 null mutation. Thymocytes from H-2b H-Y or H-2b 2C mice with or without the CD2 null mutation were stained with PE-labeled anti-CD4, FITC-labeled anti-CD8, and biotinylated MoAb to the indicated marker followed by Streptavidin Tricolor and analyzed in the FACScan flow cytometer. A total of 30,000 events were collected. The fluorescence level of the indicated molecule on gated CD4+CD8+ thymocytes with (dotted line) and without (solid line) the β2-microglobulin null mutation (β2mo) is shown.

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