Cite as: Cold Spring Harb. Protoc.; 2009; doi:10.1101/pdb.prot5345
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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
The electroporation method described here is probably the mainstay of sea squirt (Ciona) research, because the utility of transgene expression in staged embryo populations enables a wide array of biological questions to be addressed. It allows rapid identification and characterization of cis-regulatory DNA, such as tissue-specific enhancers. Electroporation of plasmids expressing fluorescent reporter genes permits live imaging and lineage tracing. Finally, structure-function relationships can be examined by expressing dominant-negative or constitutively active forms of specific proteins using appropriate cell-specific enhancers.
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