We have developed a unified, versatile vector set for expression of recombinant proteins, fit for use in any bacterial, yeast, insect or mammalian cell host. The advantage of this system is its versatility at the vector level, achieved by the introduction of a novel expression cassette. This cassette contains a unified multi-cloning site, affinity tags, protease cleavable linkers, an optional secretion signal, and common restriction endonuclease sites at key positions. This way, genes of interest and all elements of the cassette can be switched freely among the vectors, using restriction digestion and ligation without the need of polymerase chain reaction (PCR). This vector set allows rapid protein expression screening of various hosts and ...
A vector system is presented that allows generation of E. coli co-expression clones by a standardize...
<div><p>A major bottleneck in structural, biochemical and biophysical studies of proteins is the nee...
A vector system is presented that allows generation of E. coli co-expression clones by a standardize...
The expression of proteins using recombinant baculoviruses is a mature and widely used technology. H...
A vector system is presented that allows generation of E. coli co-expression clones by a standardize...
Since the number of potential drug targets identified has significantly increased in the past decade...
A vector system is presented that allows generation of E. coli co-expression clones by a standardize...
Most conditional expression vectors designed for mammalian cells have been valuable systems for stud...
Most conditional expression vectors designed for mammalian cells have been valuable systems for stud...
A new versatile mammalian vector system for protein production, cell biology analyses, and cell fact...
Protein kinases are major targets for the development of new medicines and play key roles in cellula...
Protein kinases are major targets for the development of new medicines and play key roles in cellula...
Most conditional expression vectors designed for mammalian cells have been valuable systems for stud...
Yeasts are powerful eukaryotic hosts for the production of recombinant proteins due to their rapid g...
A new versatile mammalian vector system for protein production, cell biology analyses, and cell fact...
A vector system is presented that allows generation of E. coli co-expression clones by a standardize...
<div><p>A major bottleneck in structural, biochemical and biophysical studies of proteins is the nee...
A vector system is presented that allows generation of E. coli co-expression clones by a standardize...
The expression of proteins using recombinant baculoviruses is a mature and widely used technology. H...
A vector system is presented that allows generation of E. coli co-expression clones by a standardize...
Since the number of potential drug targets identified has significantly increased in the past decade...
A vector system is presented that allows generation of E. coli co-expression clones by a standardize...
Most conditional expression vectors designed for mammalian cells have been valuable systems for stud...
Most conditional expression vectors designed for mammalian cells have been valuable systems for stud...
A new versatile mammalian vector system for protein production, cell biology analyses, and cell fact...
Protein kinases are major targets for the development of new medicines and play key roles in cellula...
Protein kinases are major targets for the development of new medicines and play key roles in cellula...
Most conditional expression vectors designed for mammalian cells have been valuable systems for stud...
Yeasts are powerful eukaryotic hosts for the production of recombinant proteins due to their rapid g...
A new versatile mammalian vector system for protein production, cell biology analyses, and cell fact...
A vector system is presented that allows generation of E. coli co-expression clones by a standardize...
<div><p>A major bottleneck in structural, biochemical and biophysical studies of proteins is the nee...
A vector system is presented that allows generation of E. coli co-expression clones by a standardize...