DNA Vectors
Invitrogen™ pTrcHis2 TOPO™ TA Expression Kit
Allow fast, efficient cloning of PCR products into prokaryotic expression vector for high-level, regulated expression from trc promoter
Invitrogen™ Vivid Colors™ pcDNA™6.2/C-YFP-DEST Vector
Allow quick and easy fusion of a protein of interest to the widely used and well-characterized fluorescent proteins from the jellyfish Aequorea victoria
Invitrogen™ pAd/PL-DEST™ Gateway™ Vector Kit
For easy recombination-based cloning and adenoviral-based, transient expression of a target gene in dividing and nondividing mammalian cells
Novus Biologicals™ N OLLAS Vector
pCMV-N OLLAS Vector for intracellular expression of N-terminally OLLAS-tagged protein
Invitrogen™ pYES2/NT A, B, & C Yeast Expression Vectors
S. cerevisiae expression vector derived from the parental pYES2 vector
MilliporeSigma™ Novagen™ pTriEx™-6 DNA
Designed to allow rapid characterization of target genes in multiple expression systems. MilliporeSigma™; Novagen™ pTriEx™-6 DNA can be used to test expression in E. coli, insect and mammalian cells.
Invitrogen™ Champion™ pET100 Directional TOPO™ Expression Kit with BL21 Star™ (DE3) One Shot™ Chemically Competent E. coli
Yields protein of interest at levels greater than 50 percent of total cellular protein in E. coli
Invitrogen™ Champion™ pET151 Directional TOPO™ Expression Kit with BL21 Star™ (DE3) One Shot™ Chemically Competent E. coli
Protein of interest can reach levels greater than 50 percent of total cellular protein during expression
Invitrogen™ Gateway™ pET-DEST42 Vector
Designed for rapid cloning with Gateway entry clone using lambda phage site-specific recombination and subsequent high-level prokaryotic expression controlled by strong bacteriophage T7 promoter
Invitrogen™ 293A Cell Line
Contains a stably integrated copy of the E1 gene that supplies the E1 proteins (E1a and E1b) required to generate recombinant adenovirus
Invitrogen™ Gateway™ pcDNA™-DEST53 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