Skip to main content
Fig. 4 | BMC Biotechnology

Fig. 4

From: Establishment of an erythroid progenitor cell line capable of enucleation achieved with an inducible c-Myc vector

Fig. 4

Induced proliferation of linTer119Mac-1Gr-1c-Kit+CD71(low/−) mouse bone marrow cells by over-expression of the transcription factor c-Myc. Shown are average measurements from 3 separate in vitro experiments where cells were modified by stable gene transfer of the TRE3G-cMyc vector, cultured in puromycin to eliminate non-modified cells (except wild type condition), then cultured with 2000 ng/ml dox for expression of the vector gene of interest or no dox as a control. Passage number and split ratio were used to determine fold expansion of total cells from the starting well and shown for 6 weeks of culture

Back to article page