METHOD OF CAS9 MEDIATED GENOME ENGINEERING

Anthony Perry; Toru Suzuki; Maki Asami

METHOD OF CAS9 MEDIATED GENOME ENGINEERING

Anthony Perry (Inventor), Toru Suzuki (Inventor), Maki Asami (Inventor)

Department of Life Sciences

Research output: Patent

Abstract

A method for altering one or more nucleic acid target sequences,comprising introducing into a first eukaryotic cell in meiosis: clustered regularly interspaced short palindromic repeats (CRISPR) associated protein 9 (Cas9) protein, or DNA or RNA encoding Cas9 (hereafter simply Cas9);and Cas9 guide RNA (gRNA) that hybridises to the target sequence(s).

Original language	English
Patent number	WO 2016/097751
IPC	A01K67/027,C12N15/10,C12N15/85,C12N15/90
Priority date	18/12/14
Filing date	18/12/15
Publication status	Published - 23 Jun 2016

Bibliographical note

1422636.9 originally entered as priority, changed to match Espacenet format

Cite this

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title = "METHOD OF CAS9 MEDIATED GENOME ENGINEERING",

abstract = "A method for altering one or more nucleic acid target sequences,comprising introducing into a first eukaryotic cell in meiosis: clustered regularly interspaced short palindromic repeats (CRISPR) associated protein 9 (Cas9) protein, or DNA or RNA encoding Cas9 (hereafter simply Cas9);and Cas9 guide RNA (gRNA) that hybridises to the target sequence(s).",

author = "Anthony Perry and Toru Suzuki and Maki Asami",

note = "1422636.9 originally entered as priority, changed to match Espacenet format; WO 2016/097751; A01K67/027,C12N15/10,C12N15/85,C12N15/90",

year = "2016",

month = jun,

day = "23",

language = "English",

type = "Patent",

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TY - PAT

T1 - METHOD OF CAS9 MEDIATED GENOME ENGINEERING

AU - Perry, Anthony

AU - Suzuki, Toru

AU - Asami, Maki

N1 - 1422636.9 originally entered as priority, changed to match Espacenet format

PY - 2016/6/23

Y1 - 2016/6/23

N2 - A method for altering one or more nucleic acid target sequences,comprising introducing into a first eukaryotic cell in meiosis: clustered regularly interspaced short palindromic repeats (CRISPR) associated protein 9 (Cas9) protein, or DNA or RNA encoding Cas9 (hereafter simply Cas9);and Cas9 guide RNA (gRNA) that hybridises to the target sequence(s).

AB - A method for altering one or more nucleic acid target sequences,comprising introducing into a first eukaryotic cell in meiosis: clustered regularly interspaced short palindromic repeats (CRISPR) associated protein 9 (Cas9) protein, or DNA or RNA encoding Cas9 (hereafter simply Cas9);and Cas9 guide RNA (gRNA) that hybridises to the target sequence(s).

UR - https://worldwide.espacenet.com/patent/search/family/054937312/publication/WO2016097751A1?q=pn%3DWO2016097751A1

M3 - Patent

M1 - WO 2016/097751

Y2 - 2015/12/18

ER -

METHOD OF CAS9 MEDIATED GENOME ENGINEERING

Abstract

Bibliographical note

Other files and links

Fingerprint

Switchable Gene Drives

Novel Homology-Directed Gene Targeting to Enhance Biomedical Modelling

MC2-Bioimaging and cell analysis

Cite this

METHOD OF CAS9 MEDIATED GENOME ENGINEERING

Abstract

Bibliographical note

Other files and links

Fingerprint

Projects

Switchable Gene Drives

Novel Homology-Directed Gene Targeting to Enhance Biomedical Modelling

Equipment

MC2-Bioimaging and cell analysis

Cite this