| 書目名稱 | Modern Applications of DNA Amplification Techniques | | 副標(biāo)題 | Problems and New Too | | 編輯 | Dirk Lassner,Barbara Pustowoit,Arndt Rolfs | | 視頻video | http://file.papertrans.cn/637/636916/636916.mp4 | | 圖書封面 |  | | 描述 | In the ten years since the first publication on PCR (Saiki et al. , 1985), this in vitro method of nucleic acid replication and modification has grown to rival in popularity traditional microbiological, genetical und technical procedures for cloning, sequencing, gene detecting and related procedures. To date the PCR literature has emphasized six main areas of application: genetic mapping, detection of mutations, genetic polymorphism, transcriptional splicing and regulation, molecular virology and quantitative procedures. The overwhelming focus of quantification of DNA or RNA by PCR has been on human microbiology and oncological problems. The exquisite sensitivity of PCR gives this method the ability to detect extremely rare DNAs, mRNAs, mRNAs in small numbers of cells or in small amounts of tissue, and mRNAs expressed in mixed-cell populations. However, the exact and accurate quantification of specific nucleic acids in biological samples is in spite of numerous publications in that field still a general problem: during the peR process, an unknown initial number of target sequences are used as a template from which a large quantity of specific product can be obtained. Although the a | | 出版日期 | Book 1997 | | 關(guān)鍵詞 | DNA; ELISA; Nucleotide; PCR; Polymerasekettenreaktion; cloning; genes; polymer; reaction; regulation; tissue; t | | 版次 | 1 | | doi | https://doi.org/10.1007/978-1-4615-5379-3 | | isbn_softcover | 978-1-4613-7455-8 | | isbn_ebook | 978-1-4615-5379-3 | | copyright | Springer Science+Business Media New York 1997 |
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