Figure 4.
Figure 4. Expression of MU3 promoter–containing lentiviral vectors in KG1a clones. (A) FACS analysis of GFP expression of single-copy clones that were identified in Figure 3 after culturing for 2 months. (B-C) Comparison of MFI values of GFP fluorescence of the single-copy KG1a clones. *The MFI values of GFP fluorescence directed by the SINF-MU3-GW-SI vector were significantly higher than those directed by the SINF-MU3-GW-I vector (P < .05, Student t test). In addition, the CV values of GFP fluorescence homogeneity obtained with the SINF-MU3-GW-SI vector (CV = 46 ± 7) were significantly better than those obtained with the SINF-MU3-GW vector (CV = 88 ± 56) (P < .05, Student t test). In panel C, thick horizontal bars represent average MFI values of GFP fluorescence as indicated by the number above each column of data points, which are denoted by individual circles.

Expression of MU3 promoter–containing lentiviral vectors in KG1a clones. (A) FACS analysis of GFP expression of single-copy clones that were identified in Figure 3 after culturing for 2 months. (B-C) Comparison of MFI values of GFP fluorescence of the single-copy KG1a clones. *The MFI values of GFP fluorescence directed by the SINF-MU3-GW-SI vector were significantly higher than those directed by the SINF-MU3-GW-I vector (P < .05, Student t test). In addition, the CV values of GFP fluorescence homogeneity obtained with the SINF-MU3-GW-SI vector (CV = 46 ± 7) were significantly better than those obtained with the SINF-MU3-GW vector (CV = 88 ± 56) (P < .05, Student t test). In panel C, thick horizontal bars represent average MFI values of GFP fluorescence as indicated by the number above each column of data points, which are denoted by individual circles.

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