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Titlebook: Decoding the Antibody Repertoire; High Throughput Sequ Brandon DeKosky Book 2017 Springer International Publishing AG 2017 B Cell.Single-ce

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發(fā)表于 2025-3-21 19:22:42 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Decoding the Antibody Repertoire
副標題High Throughput Sequ
編輯Brandon DeKosky
視頻videohttp://file.papertrans.cn/265/264402/264402.mp4
概述Nominated as an outstanding Ph.D thesis by the University of Texas at Austin.Outlines the development of the very first technology for high-throughput analysis of paired heavy and light chain antibody
叢書名稱Springer Theses
圖書封面Titlebook: Decoding the Antibody Repertoire; High Throughput Sequ Brandon DeKosky Book 2017 Springer International Publishing AG 2017 B Cell.Single-ce
描述.This thesis outlines the development of the very first technology for high-throughput analysis of paired heavy and light-chain antibody sequences, opening an entirely new window for antibody discovery and the investigation of adaptive immune responses to vaccines and diseases..Previous methods for high-throughput immune repertoire sequencing have been unable to provide information on the identity of immune receptor pairs encoded by individual B or T lymphocytes. The author directly addresses these limitations by designing two new technologies for sequencing multiple mRNA transcripts from up to 10 million isolated, single cells.. .The techniques developed in this work have enabled comprehensive interrogation of human B-cell repertoires and have been applied for rapid discovery of new human antibodies, to gain new insights into the development of human antibody repertoires, and for analysis of human immune responses to vaccination and disease..
出版日期Book 2017
關(guān)鍵詞B Cell; Single-cell Sequencing; Antibody; Immunology; Immune Repertoire; High-throughput Sequencing; Next
版次1
doihttps://doi.org/10.1007/978-3-319-58518-5
isbn_softcover978-3-319-86421-1
isbn_ebook978-3-319-58518-5Series ISSN 2190-5053 Series E-ISSN 2190-5061
issn_series 2190-5053
copyrightSpringer International Publishing AG 2017
The information of publication is updating

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Bennett T. Amaechi BDS, MS, PhDs work was undertaken specifically to address a critical deficiency in currently available high throughput antibody sequencing techniques, namely that the pairing information of heavy and light chains is irreversibly lost during traditional high-throughput sequencing. We first reported a microarray-
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發(fā)表于 2025-3-22 08:12:22 | 只看該作者
Brandon DeKoskyNominated as an outstanding Ph.D thesis by the University of Texas at Austin.Outlines the development of the very first technology for high-throughput analysis of paired heavy and light chain antibody
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發(fā)表于 2025-3-22 09:33:48 | 只看該作者
Springer Theseshttp://image.papertrans.cn/d/image/264402.jpg
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https://doi.org/10.1007/978-3-319-60961-4f VH:VL pairs is therefore currently performed by microtiter-well sorting of individual B cells followed by single-cell RT-PCR (scRT-PCR) and Sanger sequencing [.]; however at most a few hundred VH:VL pairs (a number dwarfed by the enormous size of the human antibody repertoire) are identified via scRT-PCR [.].
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https://doi.org/10.1007/978-3-319-60961-4The last 30?years of the biotechnology revolution have to a great extent been fueled by the discovery and application of monoclonal antibodies for research and therapeutic purposes.
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