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Titlebook: Citrus Tristeza Virus; Methods and Protocol Antonino F. Catara,Moshe Bar-Joseph,Grazia Licciar Book 2019 Springer Science+Business Media, L

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發(fā)表于 2025-3-21 19:02:15 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Citrus Tristeza Virus
副標題Methods and Protocol
編輯Antonino F. Catara,Moshe Bar-Joseph,Grazia Licciar
視頻videohttp://file.papertrans.cn/227/226799/226799.mp4
概述Includes cutting-edge techniques.Provides step-by-step detail essential for reproducible results.Contains key implementation advice from the experts
叢書名稱Methods in Molecular Biology
圖書封面Titlebook: Citrus Tristeza Virus; Methods and Protocol Antonino F. Catara,Moshe Bar-Joseph,Grazia Licciar Book 2019 Springer Science+Business Media, L
描述This book provides methods and clear protocols for the various technologies available to detect, characterize, and study .Citrus tristeza virus .(CTV), a member of the genus .Closterovirus., family .Closteroviridae.. Thanks to the highly sensitive and specific diagnostic procedures developed, knowledge of the molecular characteristics, expression strategies, genetic variability, and epidemiology of the virus has improved significantly, as this volume reflects. 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 and practical, .Citrus Tristeza Virus: Methods and Protocols. serves as an ideal guide for plant pathologists, plant virologists, molecular biologists, and graduate students interested in performing qualitative and quantitative tests as well as recently-developed diagnostic methods in order to find solutions to improve the management of this disease..
出版日期Book 2019
關鍵詞CTV; Plant virologists; Deep sequencing; Closterovirus; Closteroviridae; RT-PCR; Plant pathologists
版次1
doihttps://doi.org/10.1007/978-1-4939-9558-5
isbn_softcover978-1-4939-9560-8
isbn_ebook978-1-4939-9558-5Series 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

書目名稱Citrus Tristeza Virus影響因子(影響力)




書目名稱Citrus Tristeza Virus影響因子(影響力)學科排名




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書目名稱Citrus Tristeza Virus網絡公開度學科排名




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書目名稱Citrus Tristeza Virus被引頻次學科排名




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書目名稱Citrus Tristeza Virus年度引用學科排名




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A Brief Historical Account of the Family , taxon comprising plant viruses that possess very long helically constructed filamentous particles and a positive-sense single-stranded, monopartite or bipartite RNA genome and are transmitted either by aphids (genus .), pseudococcid mealybugs/soft scale insects (genus .), or whiteflies (genus .) or
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Phenotyping Biological Properties of CTV Isolates,ogical properties of a single isolate of . complex (CTV). It enables the phenotypic profile of the isolates to be defined and to infer the associated tristeza diseases (decline, seedling yellows, or stem pitting), to assess their aggressiveness or potential cross protectiveness (if any), and to moni
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Tissue-Print and Squash Capture Real-Time RT-PCR Method for Direct Detection of , (CTV) in Plant orto polymerase chain reaction (RT-PCR) neither with extract preparation nor nucleic acid purification. Immobilized CTV targets are amplified from fresh sections of plant tissues or squashes of fresh or already caught vectors onto paper, nitrocellulose, or positively charged nylon membranes. The print
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Detection of , and Coinfecting Viroids, programs require pathogen detection systems which must be economical and sensitive to maintain a healthy citrus industry. Rapid diagnostic tests for simultaneous detection of major graft-transmissible disease agents enable reduction of cost and time. The genetic and biological features of viruses a
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Assessment of Genetic Variability of , by SSCP and CE-SSCP,tes. It is a simple, low-cost, and highly specific method for mutation detection of specific genes, mostly of the CTV major coat protein gene (.). The technique is based on a comparison on polyacrylamide gel of electrophoretic profiles of single-stranded (ss) DNA sequences in terms of their spatial
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Rapid and Sensitive Detection of , Using Reverse Transcription Loop-Mediated Isothermal Amplificatil for early detection of nucleic acid targets. The LAMP technique works on the principle of strand displacement activity of . polymerase. It contains a set of four specially designed primers, which recognizes six different regions on the target nucleotide sequence. In the LAMP reaction, amplificatio
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