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CRISPR-Cas9 Ribonucleoprotein-Mediated Genomic Editing in Primary Innate Immune Cells.
Hildreth, Andrew D; Riggan, Luke; O'Sullivan, Timothy E.
Affiliation
  • Hildreth AD; Department of Microbiology, Immunology, and Molecular Genetics, David Geffen School of Medicine at UCLA, 615 Charles E. Young Drive South, BSRB 245F, Los Angeles, CA 90095, USA.
  • Riggan L; Molecular Biology Institute, University of California, Los Angeles, Los Angeles, CA 90095, USA.
  • O'Sullivan TE; Department of Microbiology, Immunology, and Molecular Genetics, David Geffen School of Medicine at UCLA, 615 Charles E. Young Drive South, BSRB 245F, Los Angeles, CA 90095, USA.
STAR Protoc ; 1(3): 100113, 2020 12 18.
Article in En | MEDLINE | ID: mdl-33377009
ABSTRACT
CRISPR-Cas9 genome engineering can be used to functionally investigate the complex mechanisms of immune system regulation. Decades of work have aimed to genetically reprogram innate immunity, but current approaches are inefficient or nonspecific, limiting their use. Here, we detail an optimized strategy for non-viral CRISPR-Cas9 ribonucleoprotein (cRNP) genomic editing of primary innate lymphocytes (ILCs) and myeloid lineage cells, resulting in high-efficiency editing of target gene expression from a single electroporation. For complete details on the use and execution of this protocol, please refer to Riggan et al. (2020).
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Electroporation / Gene Editing / Immunity, Innate Limits: Animals / Humans Language: En Journal: STAR Protoc Year: 2020 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Electroporation / Gene Editing / Immunity, Innate Limits: Animals / Humans Language: En Journal: STAR Protoc Year: 2020 Document type: Article Affiliation country: United States