Fig. 2.
Fig. 2. Detection of vector sequences in peripheral blood from baboon J95009 transplanted with CD34-enriched marrow cells transduced by 72 hours of cocultivation (LNX) in the presence of IL-3, IL-6, and SCF or over CH-296 (LN) in the presence of IL-6, SCF, FLT3L, MGDF, and protamine sulfate. (A) PCR analysis of amplified vector sequences, LNX versus LN. Standards consist of single-vector copy HT1080/LN and HT1080/LNX DNA mixed at a 1:1 ratio and then mixed with normal baboon DNA in a log dilution series. PB, peripheral blood; BM, bone marrow. (B) Percentage of vector-positive DNA measured by phosphorimage analysis of signal intensities for LN (301 bp) and LNX (326 bp) corrected for the amount of DNA as determined by actin PCR.

Detection of vector sequences in peripheral blood from baboon J95009 transplanted with CD34-enriched marrow cells transduced by 72 hours of cocultivation (LNX) in the presence of IL-3, IL-6, and SCF or over CH-296 (LN) in the presence of IL-6, SCF, FLT3L, MGDF, and protamine sulfate. (A) PCR analysis of amplified vector sequences, LNX versus LN. Standards consist of single-vector copy HT1080/LN and HT1080/LNX DNA mixed at a 1:1 ratio and then mixed with normal baboon DNA in a log dilution series. PB, peripheral blood; BM, bone marrow. (B) Percentage of vector-positive DNA measured by phosphorimage analysis of signal intensities for LN (301 bp) and LNX (326 bp) corrected for the amount of DNA as determined by actin PCR.

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