A novel low temperature PCR assured high-fidelity DNA amplification

International Journal of Molecular Sciences

Volumn 14, Issue 6, 2013, Pages 12853-12862

  Lee, Sin Hang ^a   Ge, Shichao ^b   Zhou, Shaoxia ^b   Hong, Guofan ^b  

^a Milford Hospital and Milford Molecular Laboratory   (United States)

^b INSTITUTE OF BIOCHEMISTRY AND CELL BIOLOGY   (China)

Author keywords

High processivity; High fidelity DNA amplification; LoTemp PCR; Low temperature PCR

Indexed keywords

DNA POLYMERASE; EXONUCLEASE; VIRUS DNA; DNA; PRIMER DNA; VIRUS PROTEIN;

AMPLICON; ARTICLE; CONTROLLED STUDY; DNA SEQUENCE; DNA SYNTHESIS; ENZYME ACTIVITY; HEAT TOLERANCE; HUMAN; HUMAN CELL; HUMAN PAPILLOMAVIRUS TYPE 52; LOW TEMPERATURE PROCEDURES; MOLECULAR DYNAMICS; NONHUMAN; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PROMOTER REGION; SEQUENCE ANALYSIS; VIRUS GENE; VIRUS IDENTIFICATION; VIRUS STRAIN; BASE MISPAIRING; COLD; GENETICS; KINETICS; METABOLISM; PAPILLOMAVIRIDAE; PROCEDURES;

HUMAN PAPILLOMAVIRUS TYPE 52;

BASE PAIR MISMATCH; BASE SEQUENCE; COLD TEMPERATURE; DNA; DNA PRIMERS; GENES, VIRAL; HUMANS; KINETICS; PAPILLOMAVIRIDAE; POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS, DNA; VIRAL PROTEINS;

EID: 84879378134     PISSN: 16616596     EISSN: 14220067     Source Type: Journal    
DOI: 10.3390/ijms140612853     Document Type: Article

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