In the cloning procedure we used in the lab, it is possible, albeit unlikely, for multiple inserts to form a concatamer and be cloned into a single expression vector. if three egfp inserts were cloned into a single pet-41a expression vector, would egfp be expressed (following iptg induction), and if so, would these colonies have more fluorescence compared to clones that have one copy of the egfp gene (following iptg induction)