Fig. 6.
Fig. 6. Transduction of p210BCR/ABL in NL CD34+ cells causes elevated levels of p27Kip. / Cord blood CD34+ cells (5 × 106) were transduced on 3 consecutive days with the control vector, eGFP (A: R2, eGFP−; R3, eGFP+) or with p210-eGFP (B: R3, eGFP−; R4, eGFP+). Twenty-four hours after the last transduction, cells were labeled with anti-CD34 APC, fixed, permeabilized, and incubated with antibodies against p27Kip, and washed and incubated with phycoerythrin-conjugated goat antimouse immunoglobulin. CD34+ eGFP− cells (C: R2, eGFP transduced; R4, p210-eGFP transduced) and CD34+ eGFP+ cells (D: R3, eGFP transduced; R5, p210-eGFP transduced) were gated, and p27Kip levels were compared. A representative example of 3 separate experiments is shown.

Transduction of p210BCR/ABL in NL CD34+ cells causes elevated levels of p27Kip.

Cord blood CD34+ cells (5 × 106) were transduced on 3 consecutive days with the control vector, eGFP (A: R2, eGFP; R3, eGFP+) or with p210-eGFP (B: R3, eGFP; R4, eGFP+). Twenty-four hours after the last transduction, cells were labeled with anti-CD34 APC, fixed, permeabilized, and incubated with antibodies against p27Kip, and washed and incubated with phycoerythrin-conjugated goat antimouse immunoglobulin. CD34+ eGFP cells (C: R2, eGFP transduced; R4, p210-eGFP transduced) and CD34+ eGFP+ cells (D: R3, eGFP transduced; R5, p210-eGFP transduced) were gated, and p27Kip levels were compared. A representative example of 3 separate experiments is shown.

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