I am new to CRISPR and working on a project related to glucose tolerance and insulin resistance in zebrafish. I want to knock out the gsk3α (Glycogen Synthase Kinase 3 Alpha) gene but am unfamiliar with the process. Could anyone guide me on:

  • How to select the best target sites for gsk3α knockout in zebrafish?
  • Recommended tools or software for designing sgRNA?
  • Best methods to confirm successful gene disruption?
  • Since I am a beginner, any detailed protocols, troubleshooting tips, or recommended reading materials would be greatly appreciated. Thank you!

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