Fig. 7.
Fig. 7. Globin expression analysis of EBHX11 and EBHX11L cells grown under different conditions. Cells were seeded into microtiter wells at a concentration of 30 or 100 cells per well, maintained in the indicated cytokines for 7 days, and then analyzed for βH1 and βmajor expression by Poly(A) PCR. Three samples from each set of conditions are shown. T0 represents the starting populations. Controls are the same as those in Fig 6. Expression of the ribosomal L32 gene was used as an indication of the amount of material in each lane.

Globin expression analysis of EBHX11 and EBHX11L cells grown under different conditions. Cells were seeded into microtiter wells at a concentration of 30 or 100 cells per well, maintained in the indicated cytokines for 7 days, and then analyzed for βH1 and βmajor expression by Poly(A) PCR. Three samples from each set of conditions are shown. T0 represents the starting populations. Controls are the same as those in Fig 6. Expression of the ribosomal L32 gene was used as an indication of the amount of material in each lane.

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