Rapid amplification of plasmid and phage DNA using Phi29 DNA polymerase and multiply-primed rolling circle amplification

Genome Research

Volumn 11, Issue 6, 2001, Pages 1095-1099

  Dean, Frank B ^a   Nelson, John R ^b   Giesler, Theresa L ^b   Lasken, Roger S ^a  

^a Molecular Staging Inc   (United States)

^b Amersham Biosciences   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BACTERIOPHAGE DNA; DNA POLYMERASE; NUCLEOTIDE; PHOSPHATASE; PLASMID DNA;

ARTICLE; BACTERIUM COLONY; CONTROLLED STUDY; DNA LIBRARY; DNA SEQUENCE; DNA VECTOR; GENE AMPLIFICATION; IN VITRO STUDY; MOLECULAR BIOLOGY; MOLECULAR CLONING; NONHUMAN; PRIORITY JOURNAL;

BACILLUS PHAGES; BASE SEQUENCE; DNA PRIMERS; DNA, CIRCULAR; DNA, VIRAL; DNA-DIRECTED DNA POLYMERASE; EXONUCLEASES; MOLECULAR SEQUENCE DATA; NUCLEIC ACID AMPLIFICATION TECHNIQUES; PLASMIDS; SEQUENCE ANALYSIS, DNA; TEMPLATES, GENETIC; VIRAL PROTEINS;

BACTERIA (MICROORGANISMS); UNIDENTIFIED BACTERIOPHAGE;

EID: 0034830935     PISSN: 10889051     EISSN: None     Source Type: Journal    
DOI: 10.1101/gr.180501     Document Type: Article

References (9)

1. Signal amplification of padlock probes by rolling circle replication
2. Highly efficient DNA synthesis by the phage phi 29 DNA polymerase. Symmetrical mode of DNA replication
3. Fidelity of Phi29 DNA polymerase. Comparison between protein-primed initiation and DNA polymerization
4. Rolling replication of short DNA circles
5. Rolling circle DNA synthesis: Small circular oligonucleotides as efficient templates for DNA polymerases
6. Mutation detection and single-molecule counting using isothermal rolling-circle amplification