pEGSH Vector

pEGSH Vector. Ecdysone-inducible vector, MCS contains restriction sites positioned for directional cloning of inserts derived from Lambda ZAP -derived cDNA vectors, Lambda gt10, Lambda gt11, HybridZAP vectors and other two-hybrid libraries.

To express the gene of interest, the pERV3 receptor vector and the pEGSH expression vector are part of the Complete Control Inducible Mammalian Expression System, designed to provide the tightest control of expression available in mammalian cells. The pERV3 vector contains an expression cassette from which the VgEcR and RXR proteins are constitutively expressed. Induction is fast and potent, in just 20 hours we have observed as high as 1,747-fold induction in transient assays and 1,030-fold induction in a double-stable cell line. Using a range of ponasterone A gives a linear dose response curve, allowing the amount of induction to be easily moderated.

The pERV3 vector is designed so that the genes for both VgEcR and RXR are expressed from a dicistronic message transcribed from the CMV promoter. This mode of expression was achieved by placing the internal ribosome entry site (IRES) between the VgEcR and RXR open reading frames (ORF). This construction allows efficient, high-level internal (cap-independent) initiation of translation of ORFs positioned downstream in an appropriate context. The pERV3 vector also contains a neomycin-resistance gene so that mammalian cell transfectants can be selected with the antibiotic G418.

• Dose-responsive inducible mammalian expression
• Novel IRES site allows expression of both receptor subunits from the same CMV promoter
• Induce gene expression with ponasterone A
• Unique vector design allows expression of the heterodimer receptor in a wide variety of cell lines.