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7341“…The frequency of different classes of integrons (I, II) and resistance gene cassettes (sul1,sul2, dfrA1, dfrA5 and aadB) were determined by PCR. …”
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7342“…Thus, a brief review of the advantages and disadvantages of different systems, the principles for the selection of cis elements for the expression cassettes, and available methods of plant transformation, through to the protein recovery and purification stage, are all presented here. …”
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7343“…In this study, to reduce the cumbersome hydrolysis of lovastatin to produce MJ in the native strain Aspergillus terreus, the MJ biosynthetic pathway genes (lovB, lovC, lovG, and lovA) were heterologously integrated into the genome of Aspergillus. niger CBS513.88 with strong promoters and suitable integration sites, via yeast 2μ homologous recombination to construct expression cassettes of long-length genes and CRISPR/Cas9 homology-directed recombination (CRISPR-HDR) to integrate MJ genes in the genome of A. niger. …”
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7344por Ongaro, Alfredo Edoardo, Ndlovu, Zibusiso, Sollier, Elodie, Otieno, Collins, Ondoa, Pascale, Street, Alice, Kersaudy-Kerhoas, Maïwenn“…Unfortunately, the production and disposal of single-use devices, whether in lateral flow assay, cartridges, cassettes, or lab-on-chip microfluidic format, also poses significant challenges for environmental and human health. …”
Publicado 2022
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7345por Chen, Yingying, Yang, Jiafan, Cai, Cunlei, Shi, Junjie, Song, Yongxiang, Ma, Junying, Ju, Jianhua“…Here, both pyrG and amdS-based recyclable marker cassettes were established and successfully applied in marine-derived fungi Aspergillus sp. …”
Publicado 2023
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7346“…The ubiquitous chromatin opening element (UCOE) was employed because of its ability to open chromatin and enable stable and site‐independent transgene expression. UCOE KI cassettes were randomly integrated into CHO‐K1 and HEK293T cells, followed by TI of enhanced green fluorescent protein (EGFP) onto the artificial UCOE KI site. …”
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7347“…While this has been done before, we here present an alternative sequential BioBrick assembly with the capability to accommodate many highly similar gRNA‐expression cassettes, and an exhaustive evaluation of their performance.…”
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7348“…We developed a modular cloning system that was used to easily clone a library of FAST expression cassettes in an E. coli—Thermoanaerobacter shuttle plasmid. …”
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7349por Gehlert, Finn O, Nickel, Lisa, Vakirlis, Nikolaos, Hammerschmidt, Katrin, Vargas Gebauer, Herman I, Kießling, Claudia, Kupczok, Anne, Schmitz, Ruth A“…First, mini-casposons, consisting of a R6Kγ origin and two antibiotic resistance cassettes, flanked by target site duplications (TSDs) and terminal inverted repeats (TIRs), were generated, and shown to actively translocate from a suicide plasmid and integrate into the chromosomal MetMaz-C1 TSD IS1a. …”
Publicado 2023
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7350por Yuzbashev, Tigran V., Yuzbasheva, Evgeniya Y., Melkina, Olga E., Patel, Davina, Bubnov, Dmitrii, Dietz, Heiko, Ledesma-Amaro, Rodrigo“…These include 1) A system to quickly switch between marker-free and marker-based integration constructs using both a Cre-expressing and standard Escherichia coli strains, 2) the ability to redirect multigene integration cassettes into alternative genomic loci via Golden Gate-based exchange of homology arms, 3) a rapid, simple in-vivo method to assembly guide RNA sequences via recombineering between Cas9-helper plasmids and single oligonucleotides. …”
Publicado 2023
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7351por Cochrane, Ryan R., Shrestha, Arina, Severo de Almeida, Mariana M., Agyare-Tabbi, Michelle, Brumwell, Stephanie L., Hamadache, Samir, Meaney, Jordyn S., Nucifora, Daniel P., Say, Henry Heng, Sharma, Jehoshua, Soltysiak, Maximillian P. M., Tong, Cheryl, Van Belois, Katherine, Walker, Emma J. L., Lachance, Marc-André, Gloor, Gregory B., Edgell, David R., Shapiro, Rebecca S., Karas, Bogumil J.“…In addition, we created Golden Gate assembly-compatible plasmid derivatives that allow for the generation of custom plasmids to enable the rapid insertion of designer genetic cassettes. Finally, we demonstrated that designer conjugative plasmids harboring engineered restriction endonucleases can be used as a novel antifungal agent, with important applications for the development of next-generation antifungal therapeutics.…”
Publicado 2022
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7352“…Finally, we incorporate the lambda phage recombination sites directly into an HSV-2 BAC vector for direct recombination of gene cassettes using the phage lambda clonase-driven recombination reaction. …”
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7353por Kutzleb, Christian, Sanders, Gabriele, Yamamoto, Raina, Wang, Xiaolu, Lichte, Beate, Petrasch-Parwez, Elisabeth, Kilimann, Manfred W.“…Paralemmin is highly expressed in the brain but also less abundantly in many other tissues and cell types. cDNAs from chicken, human, and mouse predict acidic proteins of 42 kD that display a pattern of sequence cassettes with high inter-species conservation separated by poorly conserved linker sequences. …”
Publicado 1998
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7354por Yamada, Ryosuke, Taniguchi, Naho, Tanaka, Tsutomu, Ogino, Chiaki, Fukuda, Hideki, Kondo, Akihiko“…RESULTS: In cocktail δ-integration, several kinds of cellulase expression cassettes are integrated into yeast chromosomes simultaneously in one step, and strains with high cellulolytic activity (i.e., expressing an optimum ratio of cellulases) are easily obtained. …”
Publicado 2010
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7355“…To study transcriptional regulation by distant enhancers, we devised a system of easilymodified reporter plasmids for integration into single-copy targeting cassettes in clones of HuH7, a human hepatocellular carcinoma. …”
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7356por Yao, Lunguang, Wang, Shanshan, Su, Shuo, Yao, Ning, He, Jian, Peng, Li, Sun, Jingchen“…A new baculovirus-silkworm multigene expression system named Bombyx mori MultiBac is developed and described here, by which multiple expression cassettes can be introduced into the Bombyx mori nuclear polyhedrosis virus (BmNPV) genome efficiently. …”
Publicado 2012
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7357“…We modified an adeno-associated virus KO shuttle vector (pTK-LoxP-NEO-AAV) to yield pAAV-LIC, which contained two cassettes at the two multiple-cloning sites. The vector was digested with EcoRV to give two fragments. …”
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7358“…They can be classified into two groups; one type is additive, that is, containing different numbers of gene cassettes, and is very variable in short time periods (they often varied even within a single CF). …”
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7359“…This is characterized by improved TALEN architecture as well as antibiotic resistance and fluorescent reporter cassettes, thus enabling enrichment for transfected cells. …”
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7360“…To determine the functionality of these promoters in constructs driving shRNA expression, anti-EGFP shRNAs (shEGFP) cassettes under the direction of bu7SK and buU6 were constructed. …”
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