Fig. 8.
Fig. 8. Bone marrow lymphoid cells differentially express the CD164(103B2/9E10) epitope. Representative dot plots from one of two separate experiments showing CD34+ bone marrow cells and Ficoll separated bone marrow mononuclear cells labeled with the 103B2/9E10 MoAb or with an IgG3 negative control MoAb plus CD34-PerCP and with the PE-conjugated MoAbs indicated before counterstaining with FITC anti-mouse IgG3 and analysis on the FACSCalibur. In contrast to the more mature CD34−CD19+ and CD34−CD20+ B cells, the immature CD34+CD19+ B-cell subset failed to express the CD164(103B2/9E10) epitope. The median fluorescence intensity for CD164(103B2/9E10) staining of the CD34−CD3+cells was 9.08 after subtraction of the isotype-matched negative control value, indicating that the CD34−CD3+ T-cell subset was weakly reactive with the 103B2/9E10 MoAb.

Bone marrow lymphoid cells differentially express the CD164(103B2/9E10) epitope. Representative dot plots from one of two separate experiments showing CD34+ bone marrow cells and Ficoll separated bone marrow mononuclear cells labeled with the 103B2/9E10 MoAb or with an IgG3 negative control MoAb plus CD34-PerCP and with the PE-conjugated MoAbs indicated before counterstaining with FITC anti-mouse IgG3 and analysis on the FACSCalibur. In contrast to the more mature CD34CD19+ and CD34CD20+ B cells, the immature CD34+CD19+ B-cell subset failed to express the CD164(103B2/9E10) epitope. The median fluorescence intensity for CD164(103B2/9E10) staining of the CD34CD3+cells was 9.08 after subtraction of the isotype-matched negative control value, indicating that the CD34CD3+ T-cell subset was weakly reactive with the 103B2/9E10 MoAb.

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