DNA Vectors
DNA Vectors
Invitrogen™ pcDNA™3.1 (+) Mammalian Expression Vector
Designed for high-level, constitutive expression in a variety of mammalian cell lines
Invitrogen™ MagicMedia™ E. coli Expression Medium
Specifically designed to dramatically increase the yield of recombinant proteins in T7-regulated E. coliexpression systems without monitoring culture O.D. (optical densities) or adding inducer
Invitrogen™ Plasmid pCMV·SPORT-βgal
Used as a positive control for monitoring expression in eukaryotic cells
Invitrogen™ ElectroMAX™ A. tumefaciens LBA4404 Cells
Agrobacterium cells that have been specially prepared for transformation by electroporation
Invitrogen™ Gateway™ pDONR™221 Vector
Enables rapid cloning of one or more genes into virtually any protein expression system
Invitrogen™ X-33, Pichia pastoris Yeast Strain
Optimize expression and recovery of protein of interest
Invitrogen™ BacMam pCMV-Dest Vector
The BacMam pCMV-Dest Vector combines Gateway™ cloning and BacMam gene expression technologies for easy recombination-based cloning and baculovirus-based expression of a target gene in variety of cell types.
Invitrogen™ GS115, Pichia pastoris Yeast Strain
Optimize expression and recovery of protein of interest
Invitrogen™ Ponasterone A
Analog of Ecdysone, insect steroid hormone that regulates metamorphosis of Drosophila melanogaster
Invitrogen™ PichiaPink™ Secreted Vector Kit
PichiaPink™ Secreted Vector Kit
Invitrogen™ pBAD TOPO™ TA Expression Kit
Specifically designed for one-step cloning and regulated prokaryotic expression of Taq-amplified PCR products
Invitrogen™ Champion™ pET SUMO Expression System
Yield high levels of protein expression in E. coli
Invitrogen™ pTrcHis2 A, B, & C Bacterial Expression Vectors
Offer enhanced translation initiation and high-level expression in E. coli
Invitrogen™ Expressway™ Mini Cell-Free Expression System
Uses efficient coupled transcription and translation reaction to produce active recombinant protein
Invitrogen™ pYES2.1 TOPO™ TA Yeast Expression Kit
Offers direct cloning of Taq-amplified PCR product into a Saccharomyces cerevisiae expression vector