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Edición del genoma mediado por CRISPR/Cas9 para el estudio de células hematopoyéticas en modelos de enfermedades
JoVE Journal
Immunology and Infection
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JoVE Journal Immunology and Infection
Lentiviral CRISPR/Cas9-Mediated Genome Editing for the Study of Hematopoietic Cells in Disease Models
DOI:

08:14 min

October 03, 2019

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Chapters

  • 00:04Title
  • 00:46Generation and Purification of Lentivirus Particles
  • 03:08Isolation and Transduction of Lineage-negative Cells from Mouse Bone Marrow
  • 05:23Transplantation of Transduced Cells into Lethally Irradiated Mice
  • 05:39Evaluating the Chimerism of Peripheral Blood
  • 06:19Results: Lentiviral Transduction of Mouse Bone Marrow Lineage-negative Cells
  • 07:23Conclusion

Summary

Automatic Translation

Se describen protocolos para la edición del genoma altamente eficiente de células madre hematopoyéticas murinas (HSPC) por el sistema CRISPR/Cas9 para desarrollar rápidamente sistemas de modelos de ratón con modificaciones genéticas específicas del sistema hematopoyético.

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