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CRISPR/Cas9 Gene Editing di cellule staminali e progenitrici ematopoietiche per applicazioni di terapia genica
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CRISPR/Cas9 Gene Editing di cellule staminali e progenitrici ematopoietiche per applicazioni di terapia genica

Article DOI: 10.3791/64064-v • 08:32 min • August 9th, 2022
August 9th, 2022 •
*1,2, *1,3, 1,2, 1,2, 1,2, 1
1Centre for Stem Cell Research (CSCR), A unit of InStem Bengaluru, Christian Medical College campus, 2Manipal Academy of Higher Education, 3Thiruvalluvar University
* These authors contributed equally

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Il presente protocollo descrive una procedura di coltura ottimizzata di cellule staminali e progenitrici ematopoietiche (HSPC) per l'attecchimento robusto di cellule geneticamente modificate in vivo.

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Biologia Numero 186
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