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Édition génique CRISPR/Cas9 de cellules souches et progénitrices hématopoïétiques pour des applications de thérapie génique
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Édition génique CRISPR/Cas9 de cellules souches et progénitrices hématopoïétiques pour des applications de thérapie génique

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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Le présent protocole décrit une procédure optimisée de culture de cellules souches et progénitrices hématopoïétiques (HSPC) pour la greffe robuste de cellules génétiquement modifiées in vivo.

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Biologie numéro 186
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