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Titlebook: Chlamydia trachomatis; Methods and Protocol Amanda Claire Brown Book 2019 Springer Science+Business Media, LLC, part of Springer Nature 201

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书目名称Chlamydia trachomatis
副标题Methods and Protocol
编辑Amanda Claire Brown
视频video
概述Includes cutting-edge techniques.Provides step-by-step detail essential for reproducible results.Contains key implementation advice from the experts
丛书名称Methods in Molecular Biology
图书封面Titlebook: Chlamydia trachomatis; Methods and Protocol Amanda Claire Brown Book 2019 Springer Science+Business Media, LLC, part of Springer Nature 201
描述This book explores cutting-edge methods to work with the notoriously difficult, but highly prevalent, obligate intracellular pathogen, .Chlamydia trachomatis.. These include techniques to identify .Chlamydia trachomatis. in patient samples, ranging from simple point-of-care tests to whole genome sequencing; methods for propagation of strains in both cell culture and animal models; techniques to manipulate .Chlamydia trachomatis .in molecular genetic methodologies; a high-throughput screening method for testing new potential drugs against intracellular bacteria; a screen for antibiotic resistance; methods for labeling and enumeration; and descriptions of genotyping technologies, as well as dual RNA-Seq transcriptional profiling. Written for the highly successful .Methods in Molecular Biology. series, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls. .Authoritative, practical, and relevant, .Chlamydia trachomatis: Methods and Protocols. serves as an ideal reference for scientists searching for a better understanding
出版日期Book 2019
关键词Drug resistance; Bacterial pathogens; Bacterium biology; Drug discovery; Treatment regimens; C; trachomat
版次1
doihttps://doi.org/10.1007/978-1-4939-9694-0
isbn_softcover978-1-4939-9696-4
isbn_ebook978-1-4939-9694-0Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightSpringer Science+Business Media, LLC, part of Springer Nature 2019
The information of publication is updating

书目名称Chlamydia trachomatis影响因子(影响力)




书目名称Chlamydia trachomatis影响因子(影响力)学科排名




书目名称Chlamydia trachomatis网络公开度




书目名称Chlamydia trachomatis网络公开度学科排名




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书目名称Chlamydia trachomatis被引频次学科排名




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书目名称Chlamydia trachomatis年度引用学科排名




书目名称Chlamydia trachomatis读者反馈




书目名称Chlamydia trachomatis读者反馈学科排名




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Antimicrobial Resistance Screening in , by Optimized McCoy Cell Culture System and Direct qPCR-Basey. Cell culture systems with immunofluorescence staining, to identify cellular inclusions in the presence of various concentrations of antimicrobial drugs, are still the most pervasive techniques, but more specific and sensitive nucleic acid concentration measuring methods are increasingly being use
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Whole-Genome Sequencing of , Directly from Human Samples,hy and mutations associated with antimicrobial resistance. The ability to sequence pathogen genomes directly from clinical specimens, without the requirement for in vitro culturing, is attractive in terms of time- and labor-saving, especially in the case of slow growing, or obligate intracellular pa
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Multilocus Sequence Typing (MLST) of ,y globally adopted as a universal fine-detailed molecular typing tool and has been applied to numerous pathogenic and nonpathogenic bacterial as well eukaryotic organisms. MLST utilizes DNA sequence of several conserved housekeeping (HK) genes which are assigned an allelic number, which then collect
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Dual RNA-Seq of Chlamydia and Host Cells,onds to the other via defense or survival strategies. Unraveling this complex interplay is key for our understanding of bacterial virulence and host response pathways for the development of novel therapeutics. Dual RNA sequencing (dual RNA-Seq) has recently been developed to simultaneously capture h
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Isolation and Propagation of Single Inclusion-Derived Chlamydia Using Laser Microdissection,dissection enables isolation of single live cells. Here we describe a method for the isolation of single .-infected cells using a laser microdissection system, in which the dissected samples are captured via gravity. Cells infected by . at low multiplicity of infection are marked with the fluorescen
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Genetic Manipulation of ,: Chromosomal Deletions,pulation of .. Valuable approaches such as random, chemically induced mutagenesis or targeted, insertion-based gene disruption have led to significant discoveries. We describe herein a technique for generating definitive null strains via complete deletion of chromosomal genes in .. Fluorescence-repo
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