Differential detection of B. pertussis from B. parapertussis using a polymerase chain reaction (PCR) in presence of SYBR green1 and amplicon melting analysis

Molecular and Cellular Probes

Volumn 18, Issue 6, 2004, Pages 429-435

  Poddar, S K ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

B. parapertussis; B. pertussis; Melting temperature (Tm); SYBR green

Indexed keywords

DNA; DOUBLE STRANDED DNA; DYE; PERTUSSIS TOXIN;

AGAR GEL ELECTROPHORESIS; AMPLICON; ARTICLE; BACTERIAL STRAIN; BACTERIUM DETECTION; BACTERIUM ISOLATION; BORDETELLA PARAPERTUSSIS; BORDETELLA PERTUSSIS; CONTROLLED STUDY; FLUORESCENCE; GENE AMPLIFICATION; MELTING POINT; NONHUMAN; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROMOTER REGION; SENSITIVITY ANALYSIS; TEMPERATURE MEASUREMENT;

BACTERIAL TYPING TECHNIQUES; BORDETELLA PARAPERTUSSIS; BORDETELLA PERTUSSIS; DNA, BACTERIAL; FLUORESCENT DYES; NUCLEIC ACID CONFORMATION; ORGANIC CHEMICALS; PHASE TRANSITION; POLYMERASE CHAIN REACTION; PROMOTER REGIONS (GENETICS); TEMPERATURE;

BORDETELLA; BORDETELLA PARAPERTUSSIS; BORDETELLA PERTUSSIS;

EID: 5644293038     PISSN: 08908508     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mcp.2004.07.003     Document Type: Article

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