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A real-time reverse-transcription PCR was developed to detect and pathotype Newcastle disease viruses (NDV) in clinical samples. Degenerate oligonucleotide primers and TaqMan probes with nonfluorescent minor groove binder (MGB) quencher amplified and hybridized to a region in the fusion protein (F) gene that corresponds to the cleavage site of the F0(More)
– A presentation of the method of Near Field Signature Analysis as a tool for diagnostic failure localization in high frequency circuit assemblies will be given. Traditional techniques of localizing faults in RF circuits rely heavily on manual methods and ATE approaches have limitations based on how much intelligence can be embedded into the software.(More)
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