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慢病毒载体平台, 用于将表观基因编辑工具高效地传递到人类诱导的多能干细胞衍生疾病模型中
JoVE Journal
Genetica
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JoVE Journal Genetica
Lentiviral Vector Platform for the Efficient Delivery of Epigenome-editing Tools into Human Induced Pluripotent Stem Cell-derived Disease Models
DOI:

13:47 min

March 29, 2019

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Capitoli

  • 00:04Titolo
  • 02:01Plasmid Design and Construction
  • 03:20HEK-293T Cells Culturing, Plating, and Transfection
  • 05:15Virus Harvesting and Viral Particles Concentrating
  • 08:16Transduction of MD NPCs
  • 09:48Analysis of Methylation Changes
  • 11:04Results: Assessment of the LV-dCas9-DNMT3A-GFP/Puro Vectors Compared to the Naive GFP Counterpart
  • 12:45Conclusion

Summary

Traduzione automatica

靶向 DNA 表观基因组编辑是一种强有力的治疗方法。该协议描述了一种一体式慢病毒载体的生产、纯化和浓度, 这些载体窝藏 CRISPR9-DNMT3A 转导基因, 用于人类诱导的多能干细胞 (hiPSC) 衍生神经元的表观基因编辑应用。

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