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1.
Nucleic Acids Res ; 39(Web Server issue): W61-7, 2011 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-21622660

RESUMEN

Uracil-Specific Exision Reagent (USER) fusion is a recently developed technique that allows for assembly of multiple DNA fragments in a few simple steps. However, designing primers for USER fusion is both tedious and time consuming. Here, we present the Primer Help for USER (PHUSER) software, a novel tool for designing primers specifically for USER fusion and USER cloning applications. We also present proof-of-concept experimental validation of its functionality. PHUSER offers quick and easy design of PCR optimized primers ensuring directionally correct fusion of fragments into a plasmid containing a customizable USER cassette. Designing primers using PHUSER ensures that the primers have similar annealing temperature (T(m)), which is essential for efficient PCR. PHUSER also avoids identical overhangs, thereby ensuring correct order of assembly of DNA fragments. All possible primers are individually analysed in terms of GC content, presence of GC clamp at 3'-end, the risk of primer dimer formation, the risk of intra-primer complementarity (secondary structures) and the presence of polyN stretches. Furthermore, PHUSER offers the option to insert linkers between DNA fragments, as well as highly flexible cassette options. PHUSER is publicly available at http://www.cbs.dtu.dk/services/phuser/.


Asunto(s)
Cartilla de ADN/química , Reacción en Cadena de la Polimerasa , Programas Informáticos , Clonación Molecular , ADN/química , Uracilo/química , Interfaz Usuario-Computador
2.
ACS Synth Biol ; 4(3): 342-9, 2015 Mar 20.
Artículo en Inglés | MEDLINE | ID: mdl-24847672

RESUMEN

USER cloning is a fast and versatile method for engineering of plasmid DNA. We have developed a user friendly Web server tool that automates the design of optimal PCR primers for several distinct USER cloning-based applications. Our Web server, named AMUSER (Automated DNA Modifications with USER cloning), facilitates DNA assembly and introduction of virtually any type of site-directed mutagenesis by designing optimal PCR primers for the desired genetic changes. To demonstrate the utility, we designed primers for a simultaneous two-position site-directed mutagenesis of green fluorescent protein (GFP) to yellow fluorescent protein (YFP), which in a single step reaction resulted in a 94% cloning efficiency. AMUSER also supports degenerate nucleotide primers, single insert combinatorial assembly, and flexible parameters for PCR amplification. AMUSER is freely available online at http://www.cbs.dtu.dk/services/AMUSER/.


Asunto(s)
Clonación Molecular/métodos , ADN/metabolismo , Mutagénesis Sitio-Dirigida/métodos , Programas Informáticos , Secuencia de Bases , ADN/química , ADN/genética , Cartilla de ADN/genética , Escherichia coli/genética , Escherichia coli/metabolismo , Internet , Datos de Secuencia Molecular , Mutación Puntual , Biología Sintética/métodos
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