STAR Protoc. 2026 Jul 7;7(3):104691.doi: 10.1016/j.xpro.2026.104691.

本文采用的英格恩产品: 电转染试剂

Protocol for generating multiplexed prime-edited monoclonal cell lines in porcine fetal fibroblasts

Affiliations

Affiliations

  • 1 National Key Laboratory for Pig Genetic Improvement and Germplasm Innovation, Ministry of Science and Technology, Jiangxi Agricultural University, Nanchang 330045, China.
  • 2 National Key Laboratory for Pig Genetic Improvement and Germplasm Innovation, Ministry of Science and Technology, Jiangxi Agricultural University, Nanchang 330045, China. Electronic address: xingyuyun9@hotmail.com.
  • 3 National Key Laboratory for Pig Genetic Improvement and Germplasm Innovation, Ministry of Science and Technology, Jiangxi Agricultural University, Nanchang 330045, China. Electronic address: wwliu199@outlook.com.

Abstract

Porcine fetal fibroblasts (PFFs) serve as standard donor cells for generating cloned pigs, and prime editing (PE) enables precise genome modification. Here, we describe a protocol for generating multiplexed prime-edited monoclonal cell lines in PFFs. We describe steps for pegRNA/ngRNA design and screening, plasmid electroporation, nocodazole treatment, puromycin selection, and monoclonal isolation and genotyping. Although demonstrated by introducing three Alzheimer’s disease-associated pathogenic mutations, the pipeline can be readily adapted to multiplex PE of other endogenous loci in porcine cells. For complete details on the use and execution of this protocol, please refer to Liu et al.1.

Keywords: Biotechnology and bioengineering; CRISPR; Genetics.

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