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CRISPR/Cas9-teknologi til genoprettelse af dystrophin-ekspression i iPSC-afledte muskel Progenitorer
JoVE Journal
Developmental Biology
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JoVE Journal Developmental Biology
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

Automatic Translation

Her præsenterer vi en Cas9-baseret exon23 sletnings protokol for at genoprette dystrofin Expression i IPSC fra DMDMDX Mouse-afledte hudfibroblaster og direkte differentiere ipscs i myogenic stamceller (MPC) ved hjælp af tet-on myod aktiveringssystem.

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