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JoVE Journal Genetics
Piattaforma di vettore lentivirale per la consegna efficiente di strumenti di editing Epigenome nelle umane indotte da modelli di malattia derivati da cellule staminali pluripotenti
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Piattaforma di vettore lentivirale per la consegna efficiente di strumenti di editing Epigenome nelle umane indotte da modelli di malattia derivati da cellule staminali pluripotenti

Article DOI: 10.3791/59241-v • 13:47 min • March 29th, 2019
March 29th, 2019 •
1,2, 3, 3, 1, 1,2, 4, 4, 1,2, 3
1Department of Neurology, Duke University Medical Center, 2Center for Genomic and Computational Biology, Duke University Medical Center, 3Viral Vector Core, Duke University Medical Center, 4Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Duke University Medical Center

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Mirati epigenome DNA modifica rappresenta un approccio terapeutico potente. Questo protocollo descrive la produzione, purificazione e concentrazione di vettori lentivirali all-in-one che harboring il transgene CRISPR-dCas9-DNMT3A per applicazioni di modifica epigenome in cellule staminali pluripotenti indotte umane (hiPSC)-derivato di neuroni.

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Genetica problema 145 vettori lentivirali DNMT3A CRISPR-dCas9 SNCA hiPSCs metilazione pyrosequencing epigenome-editing morbo di Parkinson
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