An improved, high-throughput method for detection of bluetongue virus RNA in Culicoides midges utilizing infrared-dye-labeled primers for reverse transcriptase PCR

Journal of Virological Methods

Volumn 140, Issue 1-2, 2007, Pages 140-147

  Kato, Cecilia Y ^a   Mayer, Richard T ^a  

^a USDA ARS   (United States)

Author keywords

Bluetongue virus; Culicoides sonorensis; Infrared dye; Reverse transcriptase PCR

Indexed keywords

AGAROSE; BUFFER; DYE;

ARTICLE; BLUETONGUE ORBIVIRUS; CELL CULTURE; CHEMICAL LABELING; CONTROLLED STUDY; CULICOIDES; DIAGNOSTIC ACCURACY; EPIZOOTIOLOGY; FLY; HIGH THROUGHPUT SCREENING; HOMOGENATE; INFRARED RADIATION; METHODOLOGY; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; RNA EXTRACTION; RNA PURIFICATION; RNA VIRUS; SEROTYPE; UNINDEXED SEQUENCE; VIRUS DETECTION; VIRUS ISOLATION; VIRUS STRAIN;

ANIMALS; BLUETONGUE; BLUETONGUE VIRUS; CERATOPOGONIDAE; DNA PRIMERS; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA, VIRAL; SENSITIVITY AND SPECIFICITY; SEROTYPING; TIME FACTORS;

BLUETONGUE VIRUS; CERATOPOGONIDAE; CHIRONOMIDAE; CULICOIDES SONORENSIS; EPIZOOTIC HEMORRHAGIC DISEASE VIRUS; HEXAPODA;

EID: 33846616722     PISSN: 01660934     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jviromet.2006.11.009     Document Type: Article

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