Titlebook: Rapid Methods and Automation in Microbiology and Immunology; Antti Vaheri,Richard C. Tilton,Albert Balows Book 1991 Springer-Verlag Berlin

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Q-Beta Amplification Assaysthroughout this period the patient is infectious. It is desirable to detect these agents when they are present in a low titer in order to treat infected individuals and to prevent the spread of the disease to other people. Assays that utilize nucleic acid hybridization probes (Gillespie and Spiegelm

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Phylogenetic Identification of Uncultivated Microorganisms in Natural Habitatscted so that gene sequences can be determined. However, microbiologists generally agree that at most 0.1 to 10% of microscopically observed organisms in nature can be grown axenically in the laboratory (see Atlas and Bartha 1981). The inability to culture a majority of microorganisms undoubtedly has

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rRNA Probes as Tools for Molecular Epidemiology of Microbial Infectionsion of bacteria presently relies on more or less empirical phenotypic tests. Typing is generally achieved by using special methods (i.e., different from identification methods). Current epidemiological typing systems were devised after long-term efforts and have been established for a limited set of

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Current Methods for Detection of DNA/Ribosomal RNA Hybridshylogenetic nature of the relationships which they reflect. Once the basic groundwork of nucleotide sequence analysis is laid, relatively simple hybridization experiments can rapidly track an organism or a gene across time, space, or enormous phylogenetic distance. The papers presented at this meeti

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How to Optimize Rapid and Simple Immunoassaysmprovements in immunochemical assays. Especially the use of noncompetitive assays has increased as they provide several advantages in performance and sensitivity when compared to competitive immunoassays (Ekins et al. 1985).