Fig. 2.
Fig. 2. Expression of CD8α protein and mRNA in migratory LC. / (A) DC were isolated from the draining LN 1 day after FITC painting and were stained with PE-conjugated CD8 antibody. FITC+CD8+ cells were purified using a cell sorter and were analyzed by confocal microscopy. Magnification, 60×. (B) FITC+CD8+CD11c+cells (lane 1), FITC−CD8+CD11c+ cells (lane 2), and FITC+CD8−CD11c+ cells (lane 4) were sorted to more than 90% purity from a DC-enriched population isolated from the draining LN of FITC-painted mice and were subjected to RT-PCR analysis. A suspension of total LN cells (lane 3) served as positive control. For all samples, synthesis of cDNA was controlled by RT-PCR using β-actin primers for 30 cycles. One of 3 experiments with identical results is shown.

Expression of CD8α protein and mRNA in migratory LC.

(A) DC were isolated from the draining LN 1 day after FITC painting and were stained with PE-conjugated CD8 antibody. FITC+CD8+ cells were purified using a cell sorter and were analyzed by confocal microscopy. Magnification, 60×. (B) FITC+CD8+CD11c+cells (lane 1), FITCCD8+CD11c+ cells (lane 2), and FITC+CD8CD11c+ cells (lane 4) were sorted to more than 90% purity from a DC-enriched population isolated from the draining LN of FITC-painted mice and were subjected to RT-PCR analysis. A suspension of total LN cells (lane 3) served as positive control. For all samples, synthesis of cDNA was controlled by RT-PCR using β-actin primers for 30 cycles. One of 3 experiments with identical results is shown.

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