Please cite as: CSH Protocols; 2006; doi:10.1101/pdb.prot3642
| Protocol |
This protocol was adapted from Molecular Cloning, 3rd edition, by Joseph Sambrook and David W. Russell. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, USA, 2001
| The first 15% of the full text of this article appears below. |
INTRODUCTION
In this protocol, cells transfected with a luciferase reporter plasmid are lysed in a detergent-containing buffer. Luciferase in the extract catalyzes an oxidation reaction in which D-luciferin is converted to oxyluciferin, with production of light at 556 nm that can be quantified in a luminometer.
MATERIALS
Cultured mammalian cells transfected with the DNA of interest
The cells should be transfected with a luciferase
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