DNA labeling by ligand inducible secondary structure

ChemBioChem

Volumn 9, Issue 12, 2008, Pages 1893-1897

  Peng, Tao ^a   He, Hanping ^a   Hagihara, Masaki ^a   Nakatani, Kazuhiko ^a  

^a OSAKA UNIVERSITY   (Japan)

Author keywords

Allele specific; Ligands; Mismatches; PCR; SNP typing

Indexed keywords

DNA FRAGMENT; DOUBLE STRANDED DNA; NAPHTHYRIDINE CARBAMATE DIMER; NAPHTHYRIDINE DERIVATIVE; SINGLE STRANDED DNA; UNCLASSIFIED DRUG;

ARTICLE; BASE MISPAIRING; CIRCULAR DICHROISM; DNA HYBRIDIZATION; DNA PROBE; DNA SEQUENCE; GENE AMPLIFICATION; GENE MUTATION; MOLECULAR TYPING; NUCLEIC ACID ANALYSIS; NUCLEOTIDE BINDING SITE; OLIGONUCLEOTIDE PROBE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN SECONDARY STRUCTURE; SENSITIVITY AND SPECIFICITY; SIGNAL TRANSDUCTION; SINGLE NUCLEOTIDE POLYMORPHISM; STRUCTURE ANALYSIS; TRINUCLEOTIDE REPEAT;

ALLELES; CARBAMATES; DNA; LIGANDS; NAPHTHYRIDINES; NUCLEIC ACID CONFORMATION; NUCLEIC ACID DENATURATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE NUCLEOTIDE; STAINING AND LABELING; TRANSITION TEMPERATURE;

EID: 54349128109     PISSN: 14394227     EISSN: 14397633     Source Type: Journal    
DOI: 10.1002/cbic.200800254     Document Type: Article

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37. SPR signals with match or mismatch primers almost cannot be observed for unlabeled primer (Figure S4). The signals of PCR solution were about 20 RU before PCR, only 5 RU decrease was observed after PCR.