The extremely rapid oligonucleotide hybridization and high throughput detection of microbial gene sequences using fluorescence polarization

Biosensors and Bioelectronics

Volumn 16, Issue 9-12, 2001, Pages 695-699

  Tsuruoka, Makoto ^a   Murano, Setsuko ^a   Okada, Makoto ^a   Ohiso, Isao ^a   Fujii, Takaaki ^a  

^a Adv Sci and Technology Laboratory   (Japan)

Author keywords

E. coli O157:H7; Fluorescence polarization; HCV; Hybridization rate; NaCl concentration

Indexed keywords

DNA SEQUENCES; ESCHERICHIA COLI; FLUORESCENCE; POLARIZATION; VIRUSES;

GENE SEQUENCES;

GENES;

FLUORESCENT DYE; OLIGONUCLEOTIDE; RNA; SHIGA TOXIN; SINGLE STRANDED DNA; SODIUM CHLORIDE; VEROTOXIN;

BACTERIUM DETECTION; CONFERENCE PAPER; DNA PROBE; DNA SEQUENCE; ESCHERICHIA COLI; FLUORESCENCE POLARIZATION; GENE AMPLIFICATION; GENE SEQUENCE; HEPATITIS C VIRUS; HYBRIDIZATION; MELTING POINT; NONHUMAN; POLYMERASE CHAIN REACTION; TECHNIQUE; TIME;

BASE SEQUENCE; BIOSENSING TECHNIQUES; DNA PROBES; ESCHERICHIA COLI; FLUORESCENCE POLARIZATION; GENES, BACTERIAL; GENES, VIRAL; HEPACIVIRUS; HUMANS; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; SHIGA-LIKE TOXIN I; SHIGA-LIKE TOXIN II;

EID: 0034771678     PISSN: 09565663     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0956-5663(01)00233-0     Document Type: Article

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