Fig. 6.
Fig. 6. Single-cell sorting of four subpopulations of CD34+ cord blood cells. Cord blood MNCs were stained with FITC-conjugated anti-CD34 MoAb, APC-conjugated anti-CD38 MoAb, and PE-conjugated anti–c-kit MoAb. As negative controls, FITC-, APC-, and PE-conjugated mouse IgG1 were used. (A) The lymphoblastic region (R1) was gated on the basis of FSC and SSC. (B) The gate (R2) was set on CD34+ cells. (C) The expressions of CD38 and c-kit on CD34+cells were examined. The single-cells in the R3, R4, R5, or R6 region were sorted as CD34+CD38+c-kit+, CD34+CD38+c-kit-, CD34+CD38−c-kit+, or CD34+CD38− c-kit- cells, respectively, using an automatic cell deposition unit equipped with the FACStarplus flow cytometer, as described in Materials and Methods.

Single-cell sorting of four subpopulations of CD34+ cord blood cells. Cord blood MNCs were stained with FITC-conjugated anti-CD34 MoAb, APC-conjugated anti-CD38 MoAb, and PE-conjugated anti–c-kit MoAb. As negative controls, FITC-, APC-, and PE-conjugated mouse IgG1 were used. (A) The lymphoblastic region (R1) was gated on the basis of FSC and SSC. (B) The gate (R2) was set on CD34+ cells. (C) The expressions of CD38 and c-kit on CD34+cells were examined. The single-cells in the R3, R4, R5, or R6 region were sorted as CD34+CD38+c-kit+, CD34+CD38+c-kit-, CD34+CD38c-kit+, or CD34+CD38 c-kit- cells, respectively, using an automatic cell deposition unit equipped with the FACStarplus flow cytometer, as described in Materials and Methods.

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