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CRISPR/Cas9 technologie in het herstellen van Dystrofine expressie in door iPSC afgeleide spier voorlopercellen
JoVE Journal
Biologia dello sviluppo
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JoVE Journal Biologia dello sviluppo
CRISPR/Cas9 Technology in Restoring Dystrophin Expression in iPSC-Derived Muscle Progenitors
DOI:

07:44 min

September 14, 2019

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Capitoli

  • 00:04Titolo
  • 01:45Selecting and Harvesting ES-like Cells
  • 03:02Deletion of Exon 23 in Mouse iPSCs with Two Guide RNAs (gRNAs) coupled with Cas9
  • 05:25Identification of iPSC Colonies with Exon23 Deletion
  • 06:33Results: CRISPR/Cas9-mediated Exon23 Deletion
  • 06:57Conclusion

Summary

Traduzione automatica

Hier presenteren we een Cas9-gebaseerd exon23 deletie protocol om Dystrofine expressie in iPSC te herstellen van DMDMDX Mouse-afgeleide huid fibroblasten en direct ipscs te onderscheiden in myogene voorlopercellen (MPC) met behulp van het Tet-on myod activeringssysteem.

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