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A New Reporter Vector System Based on Flow-Cytometry to Detect Promoter Activity

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Figure 1. Construction of the dual reporter vector, pRedEGFP. The  CMV promoter-driven DsRed gene, which is expressed constitutively in most mammalian cells, and the promoter-less EGFP gene are  delineated within a single vector
Figure 2. Expression of EGFP in DsRed-positive cells. (A) Promoter regions of mouse CD1d1 were cloned into the MCS of pRedEGFP and  transfected into the Bcl-1 lymphoma cell line

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