The pGL4.10[luc2], pGL4.11[luc2P] and pGL4.12[luc2CP] vectors are designed primarily to accept a putative promoter element for investigation of important regions controlling gene transcription. These promoterless vectors are available with three varieties of engineered firefly luciferase genes: luc2, luc2P or luc2CP. The inserts cloned into these vectors can easily be transferred using the multiple cloning site and a unique SfiI transfer scheme.
- Designed for cloning a putative promoter element for investigation of gene transcription control regions
- Available with three varieties of engineered firefly luciferase genes
These vectors are applicable for transcription regulation, virus-cell interactions, compound screening, post-translational modifications and promoter analysis.