← К результатам

Methods Mol Biol · 2021

Targeted Transgenic Mice Using CRISPR /Cas9 Technology.

Methods in molecular biology (Clifton, N.J.), 2214: 125-141 PMID 32944907 DOI 10.1007/978-1-0716-0958-3_9

Открыть в PubMed ↗ Открыть по DOI ↗

Аннотация

CRISPR /Cas9 is a powerful technology that has transformed gene editing of mammalian genomes, being faster and more cost-effective than standard gene targeting techniques. In this chapter, we provide a step-by-step protocol to obtain Knock-Out (KO ) or Knock-In (KI ) mouse models using CRISPR /Cas9 technology. Detailed instructions for the design of single guide RNAs (sgRNA ) for KO approaches and single-strand oligonucleotide (ssODN ) matrix for generation of KI animals are included. We also describe two independent CRISPR /Cas9 delivery methods to produce gene-edited animals starting from zygote-stage embryos, based either on cytoplasmic injection or electroporation.

Цитирование