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Rapid and Efficient Gene Deletion by CRISPR/Cas9

Title: Rapid and Efficient Gene Deletion by CRISPR/Cas9
Authors: Neldeborg, Signe; Lin, Lin; Stougaard, Magnus; Luo, Yonglun
Source: Neldeborg, S, Lin, L, Stougaard, M & Luo, Y 2019, Rapid and Efficient Gene Deletion by CRISPR/Cas9. in Methods in Molecular Biology : Methods and Protocols. Humana Press, Methods in Molecular Biology, vol. 1961, pp. 233-247. https://doi.org/10.1007/978-1-4939-9170-9_14
Publisher Information: Humana Press
Publication Year: 2019
Collection: Aarhus University: Research
Subject Terms: DNA; Deletion; Endonuclease; Gene editing; Genomic engineering; Transfection; gRNA
Description: CRISPR/Cas9 is a powerful genetic engineering technology that enables the introduction of genomic changes such as deletions and insertions of specific bits of DNA in cells with high precision. Compared to other programmable DNA nuclease such as ZFNs and TALENs, the specific binding of the Cas9 nuclease is mediated by a small guide RNA (gRNA), which can easily be designed to target any locus in the genome. The ease of generating novel gRNA vectors and its high efficiency has rapidly made CRISPR-Cas9 the dominant tool in gene editing applications, including gene knockout, knockin, tagging, etc. Here we describe our method for rapid and efficient generation of gene knockout or deletion cells using CRISPR/Cas9 within the time span of one month. The design of gRNAs, plasmid cloning, transfection, cell culturing, positive clone selection, and screening can be obtained from this method.
Document Type: book part
Language: English
Relation: info:eu-repo/semantics/altIdentifier/pmid/30912049
DOI: 10.1007/978-1-4939-9170-9_14
Availability: https://pure.au.dk/portal/en/publications/633421be-bf98-4324-a196-b21cda7b26c6; https://doi.org/10.1007/978-1-4939-9170-9_14; https://www.scopus.com/pages/publications/85063713442
Rights: info:eu-repo/semantics/restrictedAccess
Accession Number: edsbas.5B273BA6
Database: BASE