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Edição de Genes CRISPR/Cas9 de Células-Tronco Hematopoiéticas e Progenitoras para Aplicações de Terapia Gênica
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Edição de Genes CRISPR/Cas9 de Células-Tronco Hematopoiéticas e Progenitoras para Aplicações de Terapia Gênica

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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O presente protocolo descreve um procedimento de cultura otimizado de células-tronco hematopoiéticas e células progenitoras (HSPC) para o enxerto robusto de células editadas por genes in vivo.

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Biologia Edição 186
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