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Titlebook: Diagnostic Bacteriology Protocols; Louise O’Connor Book 2006Latest edition Humana Press 2006 DNA.Escherichia coli.Microarray.PCR.Single Nu

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發(fā)表于 2025-3-21 18:57:23 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書(shū)目名稱(chēng)Diagnostic Bacteriology Protocols
編輯Louise O’Connor
視頻videohttp://file.papertrans.cn/271/270644/270644.mp4
概述Includes supplementary material:
叢書(shū)名稱(chēng)Methods in Molecular Biology
圖書(shū)封面Titlebook: Diagnostic Bacteriology Protocols;  Louise O’Connor Book 2006Latest edition Humana Press 2006 DNA.Escherichia coli.Microarray.PCR.Single Nu
描述The field of bacterial diagnostics has seen unprecedented advances in recent years. The increased need for accurate detection and identification of bacteria in human, animal, food, and environmental samples has fueled the development of new techniques. The field has seen extensive research aided by the information from bacterial genome sequencing projects. Although traditional methods of bacterial detection and identification remain in use in laboratories around the world, there is now a growing trend toward the use of nucleic ac- based diagnostics and alternative biochemically and immunologically based formats. The ultimate goal of all diagnostic tests is the accurate detection, identification, or typing of microorganisms in samples of interest. Although the resulting information is of obvious use in the areas of patient management, animal health, and quality control, it is also of use in monitoring routes of infection and outlining strategies for infection control. There is, therefore, a need to ensure that the information being provided is of the highest standard and that any new technique is capable of delivering this.
出版日期Book 2006Latest edition
關(guān)鍵詞DNA; Escherichia coli; Microarray; PCR; Single Nucleotide Polymorphism; bacteria; bacteriology; hybridizati
版次2
doihttps://doi.org/10.1385/1597451436
isbn_softcover978-1-61737-666-5
isbn_ebook978-1-59745-143-7Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightHumana Press 2006
The information of publication is updating

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Use of Peptide Nucleic Acid Probes for Rapid Detection and Enumeration of Viable Bacteria in Recreaere detected by capturing chemiluminiscence on instant (e.g., Polaroid) films. Each viable cell (i.e., rRNA producing) is detected as a light spot from its microcolony on the film after scanning the image into a computer. This rapid . hybridization technique is simple and highly sensitive and could
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Detection of , in Various Sample Types Using Whole-Cell Fluorescent , Hybridization,dual cells without prior cultivation. In this chapter, the use of FISH for the detection and quantification of . in water samples and in the visualization of these bacteria inside protozoa and biofilms is described in detail.
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Macrophage Cell Cultures for Rapid Isolation of Intracellular Bacteria,ned by a flow cytometry assay for expression of . chaperonin 10. The reduced time for isolation and identification of . (48–72 h) and the consistency of the test results make the use of macrophage cell lines attractive and cost-effective for veterinary laboratories involved in surveillance of bovine
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1064-3745 ed to ensure that the information being provided is of the highest standard and that any new technique is capable of delivering this.978-1-61737-666-5978-1-59745-143-7Series ISSN 1064-3745 Series E-ISSN 1940-6029
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Book 2006Latest editionin monitoring routes of infection and outlining strategies for infection control. There is, therefore, a need to ensure that the information being provided is of the highest standard and that any new technique is capable of delivering this.
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https://doi.org/10.1007/978-3-030-03952-3dual cells without prior cultivation. In this chapter, the use of FISH for the detection and quantification of . in water samples and in the visualization of these bacteria inside protozoa and biofilms is described in detail.
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