| Literature DB >> 7543489 |
Abstract
Universal primers have been identified and a protocol developed that are suitable for rapid detection of California encephalitis (CE) complex viruses in a reverse transcription-polymerase chain reaction (RT-PCR) assay. These primers correspond to sequences in the coding regions of the G2 glycoprotein of the middle-size RNA segment. The identities of the amplified products were confirmed by sequencing on the clones or PCR products. The technique is capable of detecting 40 plaque-forming units (PFU) directly on an ethidium bromide-stained agarose gel and the sensitivity increases to 0.4-1 PFU when a radiolabeled probe is used as the detector.Entities:
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Year: 1995 PMID: 7543489 DOI: 10.1016/0166-0934(94)00176-h
Source DB: PubMed Journal: J Virol Methods ISSN: 0166-0934 Impact factor: 2.014