نتایج جستجو برای: selectable marker gene

تعداد نتایج: 1235732  

2014
Nicholas Harrison Brad Cavinder Jeffrey P. Townsend Frances Trail

Figure 1. Diagram of a split-marker gene replacement strategy using fusion-PCR (A) FPCR step 1 amplification of flanking regions and partial marker segments. Dotted tails indicate the overlap sequences on selected primers which allow fusion in step 2. (B) FPCR step 2 flanking regions are fused to the marker segments at the overlap sights, forming two constructs. The fusion products are then amp...

Journal: :Gene 1997
M Y Peredelchuk G N Bennett

A system for construction of E. coli strains with multiple DNA insertions in the chromosome, based on elements of modules for site specific recombination of Tn1545 and phage lambda, has been developed. Circular non-replicating DNA fragments containing the transposon attachment site (attTn), an excisable cassette with a selectable marker, and a gene of interest integrate randomly into the chromo...

Journal: :Plasmid 2009
Stephen R Hughes David E Sterner Kenneth M Bischoff Ronald E Hector Patrick F Dowd Nasib Qureshi Sookie S Bang Nicole Grynaviski Tania Chakrabarty Eric T Johnson Bruce S Dien Jeffrey A Mertens Robert J Caughey Siqing Liu Tauseef R Butt Joshua LaBaer Michael A Cotta Joseph O Rich

A three-plasmid yeast expression system utilizing the portable small ubiquitin-like modifier (SUMO) vector set combined with the efficient endogenous yeast protease Ulp1 was developed for production of large amounts of soluble functional protein in Saccharomyces cerevisiae. Each vector has a different selectable marker (URA, TRP, or LEU), and the system provides high expression levels of three ...

Journal: :Nucleic acids research 2004
Jan Faix Lisa Kreppel Gad Shaulsky Michael Schleicher Alan R Kimmel

Dictyostelium discoideum has proven an exceptionally powerful system for studying numerous aspects of cellular and developmental functions. The relatively small ( approximately 34 Mb) chromosomal genome of Dictyostelium and high efficiency of targeted gene disruption have enabled researchers to characterize many specific gene functions. However, the number of selectable markers in Dictyostelium...

2015
Da-Eun Jeong Seung-Hwan Park Jae-Gu Pan Eui-Joong Kim Soo-Keun Choi

Genome engineering without leaving foreign DNA behind requires an efficient counter-selectable marker system. Here, we developed a genome engineering method in Bacillus subtilis using a synthetic gene circuit as a counter-selectable marker system. The system contained two repressible promoters (B. subtilis xylA (Pxyl) and spac (Pspac)) and two repressor genes (lacI and xylR). Pxyl-lacI was inte...

Journal: :Molecular and biochemical parasitology 2002
Emmanuel Tetaud Isabelle Lecuix Tara Sheldrake Théo Baltz Alan H Fairlamb

Crithidia fasciculata is a monogenetic parasite of insects. It grows in fully defined media without requiring serum, which facilitates biochemical analysis. We have constructed a series of expression systems that allows expression of transfected genes in the kinetoplastid protozoa Crithidia and Leishmania. These cells can be readily transfected with plasmid DNA by electroporation and transforma...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2005
Asuka Nishimura Motoyuki Ashikari Shaoyang Lin Tomonori Takashi Enrique R Angeles Toshio Yamamoto Makoto Matsuoka

Regeneration of plant organs is often the essential step in genetic transformation; however, the regeneration ability of a plant varies depending on the genetic background. By conventional crosses of low-regeneration rice strain Koshihikari with high-regeneration rice strain Kasalath, we identified some quantitative trait loci, which control the regeneration ability in rice. Using a map-based c...

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