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CRISPR/Cas9 Gene Editing of Hematopoietic Stem and Progenitor Cells for Gene Therapy Applications
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CRISPR/Cas9 Gene Editing of Hematopoietic Stem and Progenitor Cells for Gene Therapy Applications

CRISPR/Cas9 Gene Editing of Hematopoietic Stem and Progenitor Cells for Gene Therapy Applications

DOI:
10.3791/64064-v

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08:32 min

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August 09, 2022

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, , , , ,
1Centre for Stem Cell Research (CSCR), A unit of InStem Bengaluru,Christian Medical College campus, 2Manipal Academy of Higher Education, 3Thiruvalluvar University

Chapters

  • 00:04Introduction
  • 00:53Gene Editing of HSPCs
  • 02:55Transplantation of Gene-Edited HSPCs
  • 04:39Assessment of Short-Term Engraftment Potential
  • 05:17Assessment of Long-Term Engraftment Potential
  • 07:01Results: Evaluating the Efficiency of CRISPR/Cas9 Gene Editing of HSPCs
  • 07:58Conclusion

Summary

자동 번역

자동 번역

The present protocol describes an optimized hematopoietic stem and progenitor cell (HSPC) culture procedure for the robust engraftment of gene-edited cells in vivo.

Tags

Keywords: CRISPR/Cas9Gene EditingHematopoietic Stem And Progenitor CellsGene TherapyEx Vivo CultureStemness PreservationMonogenic DiseasesHIVHSPC Gene Therapy ProtocolNucleofectionNSG MiceNBSGW Mice

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