Cre recombinase of bacteriophage PI has become a useful tool for molecular biological studies in vivo as well as in vitro. The Cre protein is an essential part of a system which catalyzes recombination between specific DNA sequence repeats called loxP sites. This recombination system allows for excision or inversion, depending on loxP orientation, Of DNA sequences flanked by loxP sites. In order to utilize the recombinase in mammalian systems, the retroviral vectors, LXSN and LXSHD, have been incorporated into the production of shuttle vectors and retroviral producing cell lines. The produced retroviruses allow for the transfer into and expression of the Cre recombinase in mammalian cells. These newly constructed retroviral particle...
Gene-recombinase technologies, such as Cre/loxP-mediated DNA recombination, are important tools in t...
<p>A) Schematic of the Ad5 L2 coding region. Open reading frames that encode the proteins penton (II...
For promoter studies the cloning, subcloning and transfer to different plasmid vectors usually requi...
Retroviral vectors contain viral cis-acting elements to achieve the packaging, reverse transcription...
The Cre recombinase (Cre) from bacteriophage P1 is an important tool for genetic engineering in mamm...
The Cre recombinase (Cre) from bacteriophage P1 is an important tool for genetic engineering in mamm...
Recombinant retroviruses are currently the most attractive vehicles for gene transfer into hematopoi...
PhDExpression levels of transgenes in mammalian cells show extreme variability between individual c...
Abstract Background Targeted nucleases have transformed genome editing technology, providing more ef...
The origin of the Cre recombinase gene is bacteriophage PI, and thus the codon usages are different ...
The cre-loxP-mediated recombination system (the cre-loxP system ) is an integral experimental tool ...
<p><b>Copyright information:</b></p><p>Taken from "Enhanced cell-permeant Cre protein for site-speci...
Cre-Lox recombination is known as a site-specific recombinase technology, and is widely used to carr...
Cre recombinase-mediated DNA recombination is proving to be a powerful technique for the generation ...
Murine polyomavirus is an important member of Polyomaviridae family offering potential applications ...
Gene-recombinase technologies, such as Cre/loxP-mediated DNA recombination, are important tools in t...
<p>A) Schematic of the Ad5 L2 coding region. Open reading frames that encode the proteins penton (II...
For promoter studies the cloning, subcloning and transfer to different plasmid vectors usually requi...
Retroviral vectors contain viral cis-acting elements to achieve the packaging, reverse transcription...
The Cre recombinase (Cre) from bacteriophage P1 is an important tool for genetic engineering in mamm...
The Cre recombinase (Cre) from bacteriophage P1 is an important tool for genetic engineering in mamm...
Recombinant retroviruses are currently the most attractive vehicles for gene transfer into hematopoi...
PhDExpression levels of transgenes in mammalian cells show extreme variability between individual c...
Abstract Background Targeted nucleases have transformed genome editing technology, providing more ef...
The origin of the Cre recombinase gene is bacteriophage PI, and thus the codon usages are different ...
The cre-loxP-mediated recombination system (the cre-loxP system ) is an integral experimental tool ...
<p><b>Copyright information:</b></p><p>Taken from "Enhanced cell-permeant Cre protein for site-speci...
Cre-Lox recombination is known as a site-specific recombinase technology, and is widely used to carr...
Cre recombinase-mediated DNA recombination is proving to be a powerful technique for the generation ...
Murine polyomavirus is an important member of Polyomaviridae family offering potential applications ...
Gene-recombinase technologies, such as Cre/loxP-mediated DNA recombination, are important tools in t...
<p>A) Schematic of the Ad5 L2 coding region. Open reading frames that encode the proteins penton (II...
For promoter studies the cloning, subcloning and transfer to different plasmid vectors usually requi...