Enzyme treatment-free and ligation-independent cloning using caged primers in polymerase chain reactions

Molecules

Volumn 17, Issue 1, 2012, Pages 328-340

  Kuzuya, Akinori ^a,b   Tanaka, Keita ^a   Katada, Hitoshi ^a   Komiyama, Makoto ^a  

^a UNIVERSITY OF TOKYO   (Japan)

^b KANSAI UNIVERSITY   (Japan)

Author keywords

Caged compounds; Cloning; DNA; Ligation; PCR

Indexed keywords

GREEN FLUORESCENT PROTEIN; HYBRID PROTEIN; PRIMER DNA;

ARTICLE; BIOSYNTHESIS; DNA REPAIR; ESCHERICHIA COLI; GENE VECTOR; GENETICS; METHODOLOGY; MOLECULAR CLONING; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; RADIATION EXPOSURE; SINGLE STRANDED DNA BREAK; SYNTHESIS; ULTRAVIOLET RADIATION;

BASE SEQUENCE; CLONING, MOLECULAR; DNA BREAKS, SINGLE-STRANDED; DNA PRIMERS; DNA REPAIR; ESCHERICHIA COLI; GENETIC VECTORS; GREEN FLUORESCENT PROTEINS; MOLECULAR SEQUENCE DATA; POLYMERASE CHAIN REACTION; RECOMBINANT FUSION PROTEINS; ULTRAVIOLET RAYS;

EID: 84862913447     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules17010328     Document Type: Article

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