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Flow cytometry-based quantification of targeted knock-in events in human cell lines using a GPI-anch...

Flow cytometry-based quantification of targeted knock-in events in human cell lines using a GPI-anch...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8661509

Flow cytometry-based quantification of targeted knock-in events in human cell lines using a GPI-anchor biosynthesis gene PIGP

About this item

Full title

Flow cytometry-based quantification of targeted knock-in events in human cell lines using a GPI-anchor biosynthesis gene PIGP

Publisher

England: Portland Press Ltd The Biochemical Society

Journal title

Bioscience reports, 2021-12, Vol.41 (12), p.1

Language

English

Formats

Publication information

Publisher

England: Portland Press Ltd The Biochemical Society

More information

Scope and Contents

Contents

Targeted knock-in supported by the CRISPR/Cas systems enables the insertion, deletion, and substitution of genome sequences exactly as designed. Although this technology is considered to have wide range of applications in life sciences, one of its prerequisites for practical use is to improve the efficiency, precision, and specificity achieved. To...

Alternative Titles

Full title

Flow cytometry-based quantification of targeted knock-in events in human cell lines using a GPI-anchor biosynthesis gene PIGP

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8661509

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8661509

Other Identifiers

ISSN

0144-8463

E-ISSN

1573-4935

DOI

10.1042/BSR20212231

How to access this item