期刊
APPLIED AND ENVIRONMENTAL MICROBIOLOGY
卷 67, 期 5, 页码 2384-2387出版社
AMER SOC MICROBIOLOGY
DOI: 10.1128/AEM.67.5.2384-2387.2001
关键词
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A reverse transcriptase PCR IRT-PCR) assay was developed for the detection of acute bee paralysis virus (ABPV) and black queen cell virus (BQCV), two honeybee viruses. Complete genome sequences were used to design unique PCR primers within a 1-kb region from the 3' end of both genomes to amplify a fragment of 900 bp from ABPV and 700 bp from BQCV, The combined guanidinium thiocyanate and silica membrane method was used to extract total RNA from samples of healthy and laboratory-infected bee pupae, In a blind test, RT-PCR successfully identified the samples containing ABPV and BQCV. Sensitivities were approximately 1.600 genome equivalents of purified ABPV and 130 genome equivalents of BQCV.
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