DNA Vectors

DNA vectors are molecules used as a vehicle to transfer foreign genetic material into a host cell where it can be replicated and/or expressed. These products include kits for cloning, transfection, and expression of DNA.
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To fit all of your expression needs, Invitrogen offers state-of-the-art Gateway™ destination vectors for expression in E. coli, insect, yeast, or mammalian cells, as well as for production of native protein or N- or C-terminal fusion proteins.
The pcDNA™ vectors are designed for high-level, constitutive expression in a variety of mammalian cell lines. The Gateway™ pcDNA™-DEST47 vector offers the following key features: •C-terminal Cycle 3 GFP tag for rapid detection of recombinant protein •Cytomegalovirus (CMV) promoter for high-level...
To fit all of your expression needs, Invitrogen offers state-of-the-art Gateway™ destination vectors for expression in E. coli, insect, yeast, or mammalian cells, as well as for production of native protein or N- or C-terminal fusion proteins.
Episomal iPSC Reprogramming Vectors are a cost-effective mixture of three vectors designed to provide the optimal system for generating transgene-free and virus-free induced pluripotent stem cells (iPSCs) in a feeder-free environment.
The pRABBIT IgG IRES-EmGFP Positive Control Vector is a mammalian expression control that expresses a complete, full-length rabbit IgG and EmGFP. It can be used as a positive expression control for transient expression systems such as the Expi293 Expression System, the ExpiCHO Expression System, the...
Plasmid pCMV·SPORT-bgal is used as a positive control for monitoring expression in eukaryotic cells. The plasmid contains the reporter gene b-galactosidase (b-gal) from E. coli cloned as a Not I fragment into plasmid pCMV·SPORT1.
MaV203 Competent Yeast Cells are designed for use with the ProQuest™ Two-Hybrid System (Figure 1). S. cerevisiae strain MaV203 contains deletions in the endogenous GAL4 and GAL80 genes for use with GAL4-based two-hybrid systems.
ElectroMAX™ A. tumefaciens LBA4404 Cells are Agrobacterium cells that have been specially prepared for transformation by electroporation. ElectroMAX™ LBA4404 Cells contain the disarmed Ti plasmid pAL 4404, which has only the vir and ori region of the Ti plasmid.
To fit all of your expression needs, Invitrogen offers state-of-the-art Gateway™ destination vectors for expression in E. coli, insect, yeast, or mammalian cells, as well as for production of native protein or N- or C-terminal fusion proteins.
The Baculovirus Expression System with Gateway™ Technology is designed to create recombinant pFastBac™ plasmids containing the polyhedrin promoter. The Baculovirus Expression System with Gateway™ Technology offers: • Expression using the Bac-to-Bac™ technology (1) • Destination vectors carrying the...
The pcDNA™ vectors are designed for high-level, constitutive expression in a variety of mammalian cell lines. The pcDNA3.2/V5-DEST vector offers the following key features: •Cytomegalovirus (CMV) promoter for high-level expression •attR sites for Gateway™ cloning, enabling recombination with...
The Bac-to-Bac baculovirus expression system enables the efficient production of recombinant baculovirus for expression testing in insect cells. The system relies on generation of recombinant baculovirus by site-specific transposition in E. coli rather than homologous recombination in insect cells.
To fit all of your expression needs, Invitrogen offers state-of-the-art Gateway™ destination vectors for expression in E. coli, insect, yeast, or mammalian cells, as well as for production of native protein or N- or C-terminal fusion proteins.
To fit all of your expression needs, Invitrogen offers state-of-the-art Gateway™ destination vectors for expression in E. coli, insect, yeast, or mammalian cells, as well as for production of native protein or N- or C-terminal fusion proteins.
To fit all of your expression needs, Invitrogen offers state-of-the-art Gateway™ destination vectors for expression in E. coli, insect, yeast, or mammalian cells, as well as for production of native protein or N- or C-terminal fusion proteins.
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Molecular cloning, a key component of the molecular biology workflow, is used to assemble recombinant DNA molecules and to direct their replication. In the molecular cloning workflow, the DNA to be cloned is identified and treated with enzymes to generate DNA fragments.
Lentiviral vectors are a widely used modality for gene modification in cell therapy manufacturing processes. The innovative lentivirus production solutions from Thermo Fisher Scientific are designed to accelerate and streamline the development of gene-modified cell therapies and gene therapies.
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I am interested in using the CRISPR system to modify my gene of interest using HDR instead of NHEJ repair. How can I do this?
Do I need to use the P3000 Reagent when transfecting siRNA? What if I am transfecting shRNA or miRNA in a vector?