Fig. 8.
Fig. 8. Detection of gene expression of cytokines in bone marrow of transplanted mice by RT-PCR. Bone marrow cells from Bcr-Abl–BMT mice (BMT5.1 [lanes 1 and 2], BMT5.4 [lanes 3 and 4], and BMT5.6 [lanes 5 and 6]) and a vector-BMT mouse (BMT5.35 [lanes 7 and 8]) was collected, and RNA was extracted as described in Materials and Methods. The RT-PCR products generated with (RT+) or without (RT−) reverse transcriptase were subjected to agarose gel electrophoresis, stained with ethidium bromide, and photographed by Gel Doc 1000 (Bio-Rad, Hercules, CA) with inverse gray scale. The RT-PCR products of IL-3, GM-CSF, and SCF are indicated. GAPDH was used as a control for the quality and quantity of the RNA samples and the RT-PCR reactions.

Detection of gene expression of cytokines in bone marrow of transplanted mice by RT-PCR. Bone marrow cells from Bcr-Abl–BMT mice (BMT5.1 [lanes 1 and 2], BMT5.4 [lanes 3 and 4], and BMT5.6 [lanes 5 and 6]) and a vector-BMT mouse (BMT5.35 [lanes 7 and 8]) was collected, and RNA was extracted as described in Materials and Methods. The RT-PCR products generated with (RT+) or without (RT−) reverse transcriptase were subjected to agarose gel electrophoresis, stained with ethidium bromide, and photographed by Gel Doc 1000 (Bio-Rad, Hercules, CA) with inverse gray scale. The RT-PCR products of IL-3, GM-CSF, and SCF are indicated. GAPDH was used as a control for the quality and quantity of the RNA samples and the RT-PCR reactions.

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