AbstractPreviously we established Zygote Electroporation of Nucleases (ZEN) technology as an efficient and high-throughput way to generate genetically modified mouse models. However, there were significant variations of the targeting efficiency among different genomic loci using our previously published protocol. In this study, we improved the ZEN technology by delivering Cas9 protein into mouse zygotes through a series of electroporation. Using this approach, we were able to introduce precise nucleotide substitutions, large segment deletion and short segment insertion into targeted loci with high efficiency
AbstractGene targeting in mice mainly employs homologous recombination (HR) in embryonic stem (ES) c...
Zinc finger nucleases (ZFNs) enable precise genome modification in a variety of organisms and cell t...
Despite its convenience and precision, CRISPR-based gene editing approaches still suffer from off-ta...
Previously we established Zygote Electroporation of Nucleases (ZEN) technology as an efficient and h...
CRISPR-associated (Cas) nucleases are established tools for engineering of animal genomes. These pro...
CRISPR/Cas is an adaptive immune system in bacteria and archaea that has recently been exploited for...
CRISPR/Cas9 machinery delivered as ribonucleoprotein (RNP) to the zygote has become a standard tool ...
The CRISPR/Cas9 system has been employed to efficiently edit the genomes of diverse model organisms....
<div><p>Electroporation of zygotes represents a rapid alternative to the elaborate pronuclear inject...
Electroporation of zygotes represents a rapid alternative to the elaborate pronuclear injection proc...
The CRISPR-Cas9 system in bacteria and archaea has recently been exploited for genome editing in var...
BACKGROUND: The CRISPR/Cas9 system is increasingly used for gene inactivation in mouse zygotes, but ...
International audienceThe generation of gene-edited animals using the CRISPRs/Cas9 system is based o...
<div><p>Zinc finger nucleases (ZFNs) enable precise genome modification in a variety of organisms an...
Here, we describe an expansion of the typical DNA size limitations associated with CRISPR knock-in t...
AbstractGene targeting in mice mainly employs homologous recombination (HR) in embryonic stem (ES) c...
Zinc finger nucleases (ZFNs) enable precise genome modification in a variety of organisms and cell t...
Despite its convenience and precision, CRISPR-based gene editing approaches still suffer from off-ta...
Previously we established Zygote Electroporation of Nucleases (ZEN) technology as an efficient and h...
CRISPR-associated (Cas) nucleases are established tools for engineering of animal genomes. These pro...
CRISPR/Cas is an adaptive immune system in bacteria and archaea that has recently been exploited for...
CRISPR/Cas9 machinery delivered as ribonucleoprotein (RNP) to the zygote has become a standard tool ...
The CRISPR/Cas9 system has been employed to efficiently edit the genomes of diverse model organisms....
<div><p>Electroporation of zygotes represents a rapid alternative to the elaborate pronuclear inject...
Electroporation of zygotes represents a rapid alternative to the elaborate pronuclear injection proc...
The CRISPR-Cas9 system in bacteria and archaea has recently been exploited for genome editing in var...
BACKGROUND: The CRISPR/Cas9 system is increasingly used for gene inactivation in mouse zygotes, but ...
International audienceThe generation of gene-edited animals using the CRISPRs/Cas9 system is based o...
<div><p>Zinc finger nucleases (ZFNs) enable precise genome modification in a variety of organisms an...
Here, we describe an expansion of the typical DNA size limitations associated with CRISPR knock-in t...
AbstractGene targeting in mice mainly employs homologous recombination (HR) in embryonic stem (ES) c...
Zinc finger nucleases (ZFNs) enable precise genome modification in a variety of organisms and cell t...
Despite its convenience and precision, CRISPR-based gene editing approaches still suffer from off-ta...