Improvement of φ29 DNA polymerase amplification performance by fusion of DNA binding motifs

Proceedings of the National Academy of Sciences of the United States of America

Volumn 107, Issue 38, 2010, Pages 16506-16511

  De Vega, Miguel ^a   Lázaro, José M ^a   Mencía, Mario ^a   Blanco, Luis ^a   Salas, Margarita ^a  

^a Instituto de Biología Molecular Eladio Viñuela CSIC   (Spain)

Author keywords

DNA amplification; Helix hairpin helix domain; Processivity; Protein engineering; Strand displacement

Indexed keywords

DNA POLYMERASE; GENOMIC DNA; PLASMID DNA; DNA DIRECTED DNA POLYMERASE; HYBRID PROTEIN; PRIMER DNA;

ARTICLE; CARBOXY TERMINAL SEQUENCE; CHIMERA; CONTROLLED STUDY; DNA BINDING MOTIF; DNA HAIRPIN; DNA REPLICATION; GENE AMPLIFICATION; GENE FUSION; NONHUMAN; PRIORITY JOURNAL; BACILLUS PHAGE; BINDING SITE; BIOSYNTHESIS; CHEMICAL STRUCTURE; CHEMISTRY; ENZYMOLOGY; GENETICS; METABOLISM; NUCLEIC ACID AMPLIFICATION; NUCLEOTIDE SEQUENCE; PLASMID; PROCEDURES; PROTEIN CONFORMATION; PROTEIN ENGINEERING;

BACILLUS PHAGE PHI29;

BACILLUS PHAGES; BASE SEQUENCE; BINDING SITES; DNA PRIMERS; DNA REPLICATION; DNA-DIRECTED DNA POLYMERASE; MODELS, MOLECULAR; NUCLEIC ACID AMPLIFICATION TECHNIQUES; PLASMIDS; PROTEIN CONFORMATION; PROTEIN ENGINEERING; RECOMBINANT FUSION PROTEINS;

EID: 78049312701     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1011428107     Document Type: Article

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