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Titlebook: Directed Evolution; Methods and Protocol Andrew Currin,Neil Swainston Book 2022 Springer Science+Business Media, LLC, part of Springer Natu

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樓主: Hemochromatosis
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發(fā)表于 2025-3-28 16:25:23 | 只看該作者
42#
發(fā)表于 2025-3-28 21:34:15 | 只看該作者
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發(fā)表于 2025-3-29 01:59:21 | 只看該作者
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發(fā)表于 2025-3-29 03:13:18 | 只看該作者
Antha-Guided Automation of Darwin Assembly for the Construction of Bespoke Gene Libraries,user-driven library-dependent programming of the liquid handling platform. We also present an approach for barcoding libraries that overcomes amplicon length limitations in next generation sequencing and enables fast reconstruction of library reads.
45#
發(fā)表于 2025-3-29 11:05:38 | 只看該作者
46#
發(fā)表于 2025-3-29 14:59:17 | 只看該作者
A Screening Method for P450 BM3 Mutant Libraries Using Multiplexed Capillary Electrophoresis for Dearies from directed evolution campaigns providing a comprehensive view on enzyme activity through the detection of all products formed. We describe the application of 96-MP-CE to screen mutant libraries of P450 BM3. MP-CE was used in directed evolution campaigns toward benzo-1,4-dioxane and α-isophorone.
47#
發(fā)表于 2025-3-29 18:43:49 | 只看該作者
https://doi.org/10.1007/978-3-658-02720-9binatorial-OR-type libraries based on the SpeedyGenes methodology. Together this offers a flexible platform for library synthesis, capable of generating many different bespoke, diverse libraries simultaneously.
48#
發(fā)表于 2025-3-29 22:50:30 | 只看該作者
https://doi.org/10.1007/978-3-658-02720-9 14 mutated positions, a total of 16,384 library variants, and a protocol for the generation of large, user-defined combinatorial libraries. The reader can use this protocol to create such libraries in 2 days.
49#
發(fā)表于 2025-3-30 01:37:13 | 只看該作者
50#
發(fā)表于 2025-3-30 08:04:54 | 只看該作者
https://doi.org/10.1007/978-3-322-95024-6s can be quickly and efficiently cloned into a plasmid of interest, thereby accelerating directed evolution. On top of that, PTO-QuickStep can be utilized for rapid integration of noncoding DNA fragments to modify existing plasmids, making it an excellent tool for synthetic biologists.
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