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發(fā)表于 2025-3-21 17:57:14 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Golden Gate Cloning
編輯Daniel Schindler
視頻videohttp://file.papertrans.cn/392/391116/391116.mp4
叢書名稱Methods in Molecular Biology
圖書封面Titlebook: ;
出版日期Book 2025
版次1
doihttps://doi.org/10.1007/978-1-0716-4220-7
isbn_softcover978-1-0716-4222-1
isbn_ebook978-1-0716-4220-7Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
The information of publication is updating

書目名稱Golden Gate Cloning影響因子(影響力)




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沙發(fā)
發(fā)表于 2025-3-21 23:16:47 | 只看該作者
Use of a Golden Gate Plasmid Set Enabling Scarless MoClo-Compatible Transcription Unit Assembly,erate transcription units. Typically, type IIS enzymes are used, which generate four nucleotide overhangs. This results in small scar sequences in hierarchical DNA assemblies, which can affect the functionality of transcription units. However, there are enzymes that generate three nucleotide overhan
板凳
發(fā)表于 2025-3-22 01:34:02 | 只看該作者
地板
發(fā)表于 2025-3-22 07:54:54 | 只看該作者
Validation of Golden Gate Assemblies Using Highly Multiplexed Nanopore Amplicon Sequencing,libraries, resulting in assemblies of high combinatorial complexity where sequencing again becomes mandatory. Here, we present a detailed protocol for the use of a highly multiplexed dual barcode amplicon sequencing using the Nanopore sequencing platform for in-house sequence validation. The workflo
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發(fā)表于 2025-3-22 09:47:56 | 只看該作者
Modular Golden Gate Assembly of Linear DNA Templates for Cell-Free Prototyping,tion of a repressor–promoter pair. By eliminating time-consuming transformation and cloning steps in cells and by taking advantage of modular cloning toolboxes, our cell-free prototyping workflow can produce data for large numbers of new assembled constructs within a single day.
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發(fā)表于 2025-3-22 14:29:05 | 只看該作者
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發(fā)表于 2025-3-22 18:07:44 | 只看該作者
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發(fā)表于 2025-3-22 23:33:47 | 只看該作者
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發(fā)表于 2025-3-23 03:37:40 | 只看該作者
Rosemarie Klemm,Dietrich D. Klemming the type of part that needs to be cloned, (2) designing primers for amplification, (3) performing polymerase chain reaction (PCR) amplification, (4) cloning of the fragments using Golden Gate cloning, and finally (5) sequencing of the part. For large standard parts, it is preferable to first clo
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發(fā)表于 2025-3-23 07:12:49 | 只看該作者
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