Luciferase plasmid

KP Kyrie Pappas
TM Tiphaine C. Martin
AW Andrew L. Wolfe
CN Christie B. Nguyen
TS Tao Su
JJ Jian Jin
HH Hanina Hibshoosh
RP Ramon Parsons
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The pGL3 basic reporter vector was used (as described above). See below for the sections of the PTEN promoter that were cloned into the pGL3 vector, including the restriction sites that flank each section. These constructs were made by S. Nagase in the Parsons Laboratory23 and were sequenced before performing this experiment.

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