DNA Vectors
Invitrogen™ T-REx™ Core Kit, with pcDNA™4/TO/myc-His© Vector
Tetracycline-regulated expression system without viral transactivators
Invitrogen™ pcDNA™3.1/Zeo (-) Mammalian Expression Vector
Designed for high-level, constitutive expression in a variety of mammalian cell lines
Invitrogen™ pPIC9K Pichia Vector
Carries the kanamycin resistance gene that confers resistance to Geneticin Reagent in Pichia
Invitrogen™ pEXP2-DEST Vector Kit
Destination vectors have attR sites for recombination with any attL-flanked fragment
Invitrogen™ pcDNA™3.3-TOPO™ TA Cloning™ Kit
Designed to deliver exceptionally high levels of transgene expression in adherent cells
Invitrogen™ ProBond™ Purification System
Designed for the purification of recombinant proteins that contain a polyhistidine (6xHis) sequence
Invitrogen™ Gateway™ pDEST™17 Vector
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
Invitrogen™ pBAD TOPO™ TA Expression Kit
Specifically designed for one-step cloning and regulated prokaryotic expression of Taq-amplified PCR products
Invitrogen™ Expressway™ Mini Cell-Free Expression System
Uses efficient coupled transcription and translation reaction to produce active recombinant protein
MilliporeSigma™ Novagen™ pTK-neo DNA
Used for selection of stably transfected mammalian cell lines (G418). MilliporeSigma™; Novagen™ pTK-neo DNA has a minimal thymidine kinase (TK) promoter controls expression of the neomycin resistance gene.
Invitrogen™ Gateway™ pYES-DEST52 Vector
Designed for rapid cloning with Gateway entry clone using lambda phage site-specific recombination and subsequent expression in Saccharomyces cerevisiae
Invitrogen™ pPIC6α A, B, & C Pichia Vectors
pPIC6 A, B, & C are Pichia pastoris expression vectors designed for simple selection, high-level expression, and rapid protein purification and detection.
Invitrogen™ pcDNA™3.1/V5-His TOPO™ TA Expression Kit
Provides efficient, 5-minute, one-step cloning strategy for direct insertion of Taq polymerase-amplified PCR products into plasmid vector