Cite as: Cold Spring Harb. Protoc.; 2008; doi:10.1101/pdb.prot5055
| Protocol |
Center for Regenerative and Developmental Biology, Forsyth Institute and Developmental Biology Department, Harvard School of Dental Medicine, Boston, MA 02115, USA
1Corresponding author (mlevin{at}forsyth.org)
INTRODUCTION
This protocol describes how to use the anionic membrane voltage-reporting dye DiBAC4(3) to generate images of cell membrane potential in live planarians. These images qualitatively reveal variations in time-averaged membrane potential across different regions of the organism. Changes in these images due to experimental treatments reveal how the particular treatment affects this physiological parameter. This method is a great improvement over standard electrophysiological techniques, which cannot be used to gain an understanding of the electrical properties of an entire worm or a regenerating fragment, due to small cell size and large cell number. When the proper controls are performed, this technique is a very powerful and simple way to gather physiologic data.
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