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Tecnología CRISPR/Cas9 en la restauración de la expresión de distrofina en progenitores musculares derivados de iPSC
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CRISPR/Cas9 Technology in Restoring Dystrophin Expression in iPSC-Derived Muscle Progenitors
DOI:

07:44 min

September 14, 2019

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Chapters

  • 00:04Title
  • 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

자동 번역

Aquí, presentamos un protocolo de eliminación exon23 basado en Cas9 para restaurar la expresión de distrofina en iPSC a partir de fibroblastos cutáneos derivados del ratón Dmdmdx y diferenciar directamente los iPSC en células progenitoras miogénicas (MPC) utilizando el sistema de activación Tet-on MyoD.

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