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Updated: Feb 7, 2026

Chromatin Immunoprecipitation Assay for Tissue-specific Genes using Early-stage Mouse Embryos
Published on: April 29, 2011
Time Matters: Gene Editing at the Mouse 2-Cell Embryo Stage Boosts Knockin Efficiency
Alvaro Plaza Reyes1, Fredrik Lanner1
1Department of Clinical Science, Intervention and Technology, Karolinska Institutet, 14186 Stockholm, Sweden; Ming Wai Lau Center for Reparative Medicine, Karolinska Institutet, 14186 Stockholm, Sweden; Division of Obstetrics and Gynecology, Karolinska Universitetssjukhuset, 14186 Stockholm, Sweden.
Abstract:
Although endonuclease-mediated genome editing techniques offer significant improvement over traditional methods, they are still ineffective for introduction of large DNA sequences. Recently in Nature Biotechnology, Gu et al. (2018) developed a CRISPR-Cas strategy termed 2C-HR-CRISPR that generates fluorescent reporter tagging of genes with up to 95% knockin efficiency in mouse embryos.
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According to its composition, the matter can be classified into two broad categories — pure substances and mixtures.
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