The CCTL (Cpf1-assisted Cutting and Taq DNA ligase-assisted Ligation) method for efficient editing of large DNA constructs in vitro

Nucleic Acids Research

Volumn 45, Issue 9, 2017, Pages

  Lei, Chao ^a   Li, Shi Yuan ^a,b   Liu, Jia Kun ^a,b   Zheng, Xuan ^a,b   Zhao, Guo Ping ^a,b,c,d   Jin, Wang ^a  

^a INSTITUTE OF PLANT PHYSIOLOGY AND ECOLOGY   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

^c FUDAN UNIVERSITY   (China)

^d CHINESE UNIVERSITY OF HONG KONG   (Hong Kong)

Author keywords

[No Author keywords available]

Indexed keywords

ACTINORHODINE; CPF1 PROTEIN; CRISPR ASSOCIATED PROTEIN; CRRNA; DNA LIGASE; RNA; UNCLASSIFIED DRUG; DNA; TAQ POLYMERASE;

ACTII ORF4 GENE; ARTICLE; BIOSYNTHESIS; CONTROLLED STUDY; CPF1 ASSISTED CUTTING AND TAQ DNA LIGASE ASSISTED LIGATION; GENE; GENE CONSTRUCT; GENE EDITING; GENE EXPRESSION; GENE TARGETING; GENETIC ENGINEERING; IN VITRO STUDY; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN CLEAVAGE; PROTEIN MOTIF; RNA STRUCTURE; ENZYMOLOGY; FRANCISELLA; METABOLISM;

CRISPR-ASSOCIATED PROTEINS; DNA; FRANCISELLA; TAQ POLYMERASE;

EID: 85027284460     PISSN: 03051048     EISSN: 13624962     Source Type: Journal    
DOI: 10.1093/nar/gkx018     Document Type: Article

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