Table 1.

Analysis of expression of clones from stable cell lines

Cell typeConstructClones expressing the
reporter/total clones
with transgene
U937 human myeloid (PU.1+Dnase I HS + PU.1
promoter 
14/14  
U937 human myeloid (PU.1+PU.1 promoter only 10/14  
416B murine myeloid (PU.1+Dnase I HS + PU.1
promoter 
18/18 
416B murine myeloid (PU.1+PU.1 promoter only 14/16  
BW5147 murine T cell (PU.1Dnase I HS + PU.1
promoter 
18/18  
BW5147 murine T cell (PU.1PU.1 promoter only 15/18 
Cell typeConstructClones expressing the
reporter/total clones
with transgene
U937 human myeloid (PU.1+Dnase I HS + PU.1
promoter 
14/14  
U937 human myeloid (PU.1+PU.1 promoter only 10/14  
416B murine myeloid (PU.1+Dnase I HS + PU.1
promoter 
18/18 
416B murine myeloid (PU.1+PU.1 promoter only 14/16  
BW5147 murine T cell (PU.1Dnase I HS + PU.1
promoter 
18/18  
BW5147 murine T cell (PU.1PU.1 promoter only 15/18 

Clones were considered to be expressing the reporter if luciferase activity was 3-fold higher than background. The luciferase activity of the average of expressing clones is shown in Figure4B.

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