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. 2000 Sep 1;28(17):e79. doi: 10.1093/nar/28.17.e79

Figure 1.

Figure 1

PCR analysis of recombinant clones with primers LUG1 and LUG2. The parent clone (lane 1) gives a 440 bp product, while insertion of the TetR cassette into the β-globin gene yields a 1830 bp product (lane 2). Deletion of the TetR gene after a second round of recombination with a PCR fragment carrying only the IVS I-110 mutation in the β-globin gene restores the original PCR product size (lanes 3 and 4).