Targeted Mutations in the Mouse via Embryonic Stem Cells

Genetic modification of mouse embryonic stem (ES) cells is a powerful technology that enabled the generation of a plethora of mutant mouse lines to study gene function and mammalian biology. Here we describe ES cell culture and transfection techniques used to manipulate the ES cell genome to obtain targeted ES cell clones. We include the standard gene targeting approach as well as the application of the CRISPR/Cas9 system that can improve the efficiency of homologous recombination in ES cells by introducing a double-strand DNA break at the target site.

Medienart:

E-Artikel

Erscheinungsjahr:

2020

Erschienen:

2020

Enthalten in:

Zur Gesamtaufnahme - volume:2066

Enthalten in:

Methods in molecular biology (Clifton, N.J.) - 2066(2020) vom: 01., Seite 59-82

Sprache:

Englisch

Beteiligte Personen:

Gertsenstein, Marina [VerfasserIn]
Mianné, Joffrey [VerfasserIn]
Teboul, Lydia [VerfasserIn]
Nutter, Lauryl M J [VerfasserIn]

Links:

Volltext

Themen:

CRISPR associated protein (Cas9)
Clustered regularly interspaced short palindromic repeats (CRISPR)
Electroporation
Embryonic stem (ES) cells
Gene targeting
Journal Article
Mouse
RNA, Guide, CRISPR-Cas Systems

Anmerkungen:

Date Completed 14.12.2020

Date Revised 04.01.2024

published: Print

Citation Status MEDLINE

doi:

10.1007/978-1-4939-9837-1_5

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM301208220