Fig. 6.
Fig. 6. Effect of IK antisense oligonucleotides on HLA-DR and CD34 antigen expression by cord blood CD34+ cells. Isolated CD34+ cells were cultured in IMDM containing 5% FCS and a combination of 3 cytokines, IL-1, IL-3, and SCF, in the presence of IK antisense or control oligonucleotides. After 7 days of culture, cells were collected and stained either with antihuman FITC-conjugated anti-HLA-DR MoAb or PE-conjugated anti-CD34+ MoAb (━) or with negative control antibodies (─). (A and E) Freshly isolated CD34+ cells (day 0) CD34+ cells cultured for 7 days either in the absence of oligonucleotide (B and F ) or in the presence of control (20 μmol/L) (C and G) or antisense (20 μmol/L) (D and H) oligonucleotides.

Effect of IK antisense oligonucleotides on HLA-DR and CD34 antigen expression by cord blood CD34+ cells. Isolated CD34+ cells were cultured in IMDM containing 5% FCS and a combination of 3 cytokines, IL-1, IL-3, and SCF, in the presence of IK antisense or control oligonucleotides. After 7 days of culture, cells were collected and stained either with antihuman FITC-conjugated anti-HLA-DR MoAb or PE-conjugated anti-CD34+ MoAb (━) or with negative control antibodies (─). (A and E) Freshly isolated CD34+ cells (day 0) CD34+ cells cultured for 7 days either in the absence of oligonucleotide (B and F ) or in the presence of control (20 μmol/L) (C and G) or antisense (20 μmol/L) (D and H) oligonucleotides.

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