Fig. 2.
Fig. 2. Isolation of CD8α+CD11c−Lin− cells from BM and lymph nodes. / BM cells (A) and lymph node cells (combined axillary, cervical, inguinal, and mesenteric lymph nodes; B) were enriched by CD8α-microbeads and then stained with biotin-conjugated anti-CD11c, revealed with APC-streptavidin, as well as FITC-conjugated anti-CD8α, PE-conjugated anti-Lin markers (CD3ε, B220, Gr-1, CD11b, and NK1.1). The CD8α versus Lin markers staining was gated on CD11c−cells. The gate indicated the BM-derived (A) and lymph node–derived (B) CD8α+CD11c−Lin− cells, respectively. The results are representative of 3 independent experiments.

Isolation of CD8α+CD11cLin cells from BM and lymph nodes.

BM cells (A) and lymph node cells (combined axillary, cervical, inguinal, and mesenteric lymph nodes; B) were enriched by CD8α-microbeads and then stained with biotin-conjugated anti-CD11c, revealed with APC-streptavidin, as well as FITC-conjugated anti-CD8α, PE-conjugated anti-Lin markers (CD3ε, B220, Gr-1, CD11b, and NK1.1). The CD8α versus Lin markers staining was gated on CD11ccells. The gate indicated the BM-derived (A) and lymph node–derived (B) CD8α+CD11cLin cells, respectively. The results are representative of 3 independent experiments.

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