Published March 15, 2018 | Version Accepted Version
Book Section - Chapter Open

CRISPR Knockouts in Ciona Embryos

  • 1. ROR icon New York University
  • 2. ROR icon California Institute of Technology
  • 3. ROR icon Georgia Institute of Technology

Contributors

Abstract

Clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9 has emerged as a revolutionary tool for fast and efficient targeted gene knockouts and genome editing in almost any organism. The laboratory model tunicate Ciona is no exception. Here, we describe our latest protocol for the design, implementation, and evaluation of successful CRISPR/Cas9-mediated gene knockouts in somatic cells of electroporated Ciona embryos. Using commercially available reagents, publicly accessible plasmids, and free web-based software applications, any Ciona researcher can easily knock out any gene of interest in their favorite embryonic cell lineage.

Additional Information

© 2018 Springer Nature Singapore Pte Ltd. First Online: 15 March 2018. Research in the laboratory of L.C. is supported by R01 awards HL108643 and GM096032 from the NIH/NHLBI and NIH/NIGMS respectively; and by grant 15CVD01 from the Leducq Foundation. A.S. is supported by R00 award HD084814 from the NIH/NICHD.

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Accepted Version - nihms-976213.pdf

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Additional details

Identifiers

PMCID
PMC6061950
Eprint ID
85358
Resolver ID
CaltechAUTHORS:20180319-130924469

Funding

NIH
HL108643
NIH
GM096032
Leducq Foundation
15CVD01
NIH
HD084814

Dates

Created
2018-03-26
Created from EPrint's datestamp field
Updated
2021-11-15
Created from EPrint's last_modified field

Caltech Custom Metadata

Series Name
Advances in Experimental Medicine and Biology
Series Volume or Issue Number
1029