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. 2018 May 4;16(1):137–144. doi: 10.3892/ol.2018.8638

Figure 3.

Figure 3.

Recombination of pGL3-DKK1-5-TREs. (A) The location and order of TREs, HS2, DKK1-5 and luciferase in the constructs. The candidate TREs were cloned in front of a DKK1-5 promoter-driven luciferase reporter pGL3-basic vector. (B) Identification of reconstructed TRE reporter plasmids by restriction enzyme digestion. The position on the 1.0% agarose gel corresponds to the specific TRE, as indicated. DKK1, dickkopf 1; TRE, transcriptional regulatory element; HS2, DNase I hypersensitive site II; Poly-A, polyadenylated tail; LUC, luciferase.