Related Experiment Video
Updated: Jun 24, 2026

In vivo Dual Substrate Bioluminescent Imaging
Published on: October 11, 2011
A bioluminescent enzyme immunoassay for prostaglandin E(2) using Cypridina luciferase
Chun Wu1, Saki Irie, Shozo Yamamoto
1Research Institute for Cell Engineering, National Institute of Advanced Industrial Science and Technology, Osaka 563-8577, Japan. chun-wu@aist.go.jp
Abstract:
Prostaglandin E(2) is one of the major cyclooxygenase metabolites of arachidonic acid. We developed a competitive immunosorbent assay for prostaglandin E(2) utilizing a bioluminescent enzyme Cypridina luciferase. The prostaglandin E(2) amount could be quantified over the concentration ranging from 7.8 to 500 pg/mL. The amount of unlabeled prostaglandin E(2) required to displace 50% of the maximal binding of Cypridina luciferase-labeled prostaglandin E(2) (B/B(0)) was approximately 35 pg/mL. The results show a great potential of Cypridina luciferase as a new labeling enzyme for enzyme-linked immunosorbent assay.
More Related Videos
10:33Flexible Measurement of Bioluminescent Reporters Using an Automated Longitudinal Luciferase Imaging Gas- and Temperature-optimized Recorder (ALLIGATOR)
Published on: December 13, 2017
10:38Monitoring Cell-autonomous Circadian Clock Rhythms of Gene Expression Using Luciferase Bioluminescence Reporters
Published on: September 27, 2012