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Titlebook: Combinatorial Peptide Library Protocols; Shmuel Cabilly Book 1998 Humana Press 1998

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發(fā)表于 2025-3-21 19:03:16 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Combinatorial Peptide Library Protocols
編輯Shmuel Cabilly
視頻videohttp://file.papertrans.cn/231/230011/230011.mp4
叢書名稱Methods in Molecular Biology
圖書封面Titlebook: Combinatorial Peptide Library Protocols;  Shmuel Cabilly Book 1998 Humana Press 1998
描述During the course of evolution, an imbalance was created between the rate of vertebrate genetic adaptation and that of the lower forms of living organisms, such as bacteria and viruses. This imbalance has given the latter the advantage of generating, relatively quickly, molecules with unexpected structures and features that carry a threat to vertebrates. To compensate for their weakness, vertebrates have accelerated their own evolutionary processes, not at the level of whole organism, but in specialized cells containing the genes that code for antibody molecules or for T-cell receptors. That is, when an immediate requirement for molecules capable of specific interactions arose, nature has preferred to speed up the mode of Darwinian evolution in pref- ence to any other approach (such as the use of X-ray diffraction studies and computergraphic analysis). Recently, Darwinian rules have been adapted for test tube research, and the concept of selecting molecules having particular characteristics from r- dom pools has been realized in the form of various chemical and biological combinatorial libraries. While working with these libraries, we noticed the interesting fact that when combinat
出版日期Book 1998
版次1
doihttps://doi.org/10.1385/0896033929
isbn_softcover978-1-61737-022-9
isbn_ebook978-1-59259-571-6Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightHumana Press 1998
The information of publication is updating

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沙發(fā)
發(fā)表于 2025-3-21 23:47:34 | 只看該作者
Smart Learning with Educational Roboticsxpression systems have been developed in order to construct such libraries containing tens to hundreds of mlllions of random peptlde sequences that can be screened for their abihty to bind particular antibodies (.). In essence these phage-expressed peptides mimic the determinants of the antigen that are recognized by the antibodies.
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https://doi.org/10.1007/978-3-031-54207-7 same compound in and on the same bead (.–.). With an appropriate detection scheme, compound-beads with specific biological, physical, or chemical properties can be identified, and physically isolated, and then their chemical structure can be determined. In biological systems, one important property
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https://doi.org/10.1007/978-3-031-54207-7ing blocks used are represented. The development and verification of the utility of combinatorial libraries represent a dramatic advance in the drug discovery process by greatly reducing the time needed to identify new drug leads. Positional scanning (PS) SCLs (.,.) represent a modified format of th
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https://doi.org/10.1007/978-3-031-54207-7 detection of epitopes as well as for the identification of peptides that act as antagonists of medically relevant proteins. We have prepared different types of cellulose-bound peptide libraries by spot synthesis (.), which is a powerful tool for the simultaneous and positionally addressable synthes
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Authoring Tools to Design Smart LOscommercially available bis-2-aminopropyl-PEG.. With the use of this PEG., permeability with proteins up to 50 kDa has been achieved, as demonstrated by gel permeation chromatography (.). A resin-bound fluoroescencequenched peptide substrate showed 80% cleavage with subtihsin Carlsberg (MW 27 kDa) in
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