Technique for quantitative detection of specific DNA sequences using alternately binding quenching probe competitive assay combined with loop-mediated isothermal amplification

Analytical Chemistry

Volumn 79, Issue 15, 2007, Pages 5608-5613

  Tani, Hidenori ^a,b   Teramura, Tatsuya ^a,b   Adachi, Ken ^a,b   Tsuneda, Satoshi ^a   Kurata, Shinya ^c   Nakamura, Kazunori ^b,d   Kanagawa, Takahiro ^e   Noda, Naohiro ^b  

^a WASEDA UNIVERSITY   (Japan)

^b NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY AIST   (Japan)

^c J Bio 21 Corporation   (Japan)

^d UNIVERSITY OF TSUKUBA   (Japan)

^e Ukyo ku   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

BINDING QUENCHING; FLUORESCENCE INTENSITY; ISOTHERMAL AMPLIFICATION;

BINDING ENERGY; BIOASSAY; FLUORESCENCE; GENES; ISOTHERMS; OLIGONUCLEOTIDES;

DNA SEQUENCES;

BACTERIAL DNA; FLUORESCENT DYE; HUMIC ACID; OLIGONUCLEOTIDE; OXIDOREDUCTASE; PROTEIN AMOA; TRITON X 100; UNCLASSIFIED DRUG; UREA;

ACCURACY; ALTERNATELY BINDING QUENCHING PROBE COMPETITIVE ASSAY; AMOA GENE; ARTICLE; CALCULATION; DNA DETERMINATION; DNA PROBE; DNA SEQUENCE; FLUORESCENCE; GENE; GENE AMPLIFICATION; ISOTHERM; LOOP MEDIATED ISOTHERMAL AMPLIFICATION; NITROSOMONAS EUROPAEA; NONHUMAN; QUANTITATIVE ANALYSIS; REACTION ANALYSIS; REAL TIME POLYMERASE CHAIN REACTION; STANDARD; TURBIDIMETRY;

BASE SEQUENCE; BINDING, COMPETITIVE; DNA; DNA PROBES; FLUORESCENT DYES; HUMIC SUBSTANCES; MOLECULAR SEQUENCE DATA; NEPHELOMETRY AND TURBIDIMETRY; NUCLEIC ACID AMPLIFICATION TECHNIQUES; OCTOXYNOL; OXIDOREDUCTASES; POLYMERASE CHAIN REACTION; REPRODUCIBILITY OF RESULTS; RNA, BACTERIAL; SENSITIVITY AND SPECIFICITY; SEQUENCE ANALYSIS, DNA; TEMPERATURE; UREA;

EID: 34547728059     PISSN: 00032700     EISSN: None     Source Type: Journal    
DOI: 10.1021/ac070041e     Document Type: Article

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