Effect of DNA damage on PCR amplification efficiency with the relative threshold cycle method

Biochemical and Biophysical Research Communications

Volumn 323, Issue 3, 2004, Pages 823-830

  Sikorsky, Jan A ^a   Primerano, Donald A ^a   Fenger, Terry W ^a   Denvir, James ^a,b  

^a MARSHALL UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b MARSHALL UNIVERSITY   (United States)

Author keywords

Amplification efficiency; Base modification; DNA damage; Real time PCR; Taq polymerase

Indexed keywords

8 HYDROXYDEOXYGUANOSINE; THYMIDINE;

ARTICLE; CIS ISOMER; CONTROLLED STUDY; CORRELATION ANALYSIS; CYCLIZATION; DIMERIZATION; DNA DAMAGE; DNA MODIFICATION; DNA TEMPLATE; ENZYME ASSAY; GENE AMPLIFICATION; HUMAN; MOLECULAR DYNAMICS; MOLECULAR INTERACTION; MOLECULAR MECHANICS; PHASE SEPARATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; STATISTICAL SIGNIFICANCE; TECHNIQUE;

BASE PAIR MISMATCH; BASE SEQUENCE; COMBINATORIAL CHEMISTRY TECHNIQUES; DNA DAMAGE; DNA REPLICATION; MOLECULAR SEQUENCE DATA; OLIGONUCLEOTIDES; POLYMERASE CHAIN REACTION; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 4544356659     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbrc.2004.08.168     Document Type: Article

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