Cite as: Cold Spring Harb. Protoc.; 2009; doi:10.1101/pdb.prot5346
| Protocol |
Molecular and Cell Biology Department, University of California, Berkeley, California 94720, USA
1 Present address: Center for Developmental Genetics, Department of Biology, Faculty of Arts and Science, New York University, New York, NY 10003, USA.
2Corresponding authors (mlevine{at}berkeley.edu); (lc121{at}nyu.edu).
INTRODUCTION
This protocol describes the fixation, staining, and mounting of sea squirt (Ciona intestinalis) embryos and larvae that have been electroporated with a plasmid DNA containing a cis-regulatory DNA (e.g., tissue-specific enhancer) fused to the lacZ reporter gene. Green fluorescent protein (GFP) reporter genes can be directly visualized in living embryos and larvae, although fixed preparations can use aspects of this protocol.
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