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The iDimerize Inducible Heterodimer System can be used to create and control specific interactions between two different proteins. The proteins of interest are fused to the DmrA and DmrC binding domains, respectively, and dimerization is induced by adding the cell-permeant ligand A/C Heterodimerizer (identical to the AP21967 ligand) to the culture medium or by administering it in vivo. Plasmid and lentiviral (Lenti-X) vector formats are available.
The iDimerize Inducible Heterodimer System can be used to create and control specific interactions between two different proteins. The proteins of interest are fused to the DmrA and DmrC binding domains, respectively, and dimerization is induced by adding the cell permeant ligand A/C Heterodimerizer (identical to the AP21967 ligand) to the culture medium or by administering it in vivo. Plasmid and lentiviral (Lenti-X) vector formats are available.
iDimerize Inducible Heterodimer System (with Tet-On 3G technology)
One challenge of ligand-dependent dimerization experiments is that non-ligand-induced dimerization events may occur if the proteins of interest are expressed at high levels. This is especially problematic if the target proteins are membrane-bound, because the local concentrations can increase quickly due to the limited space on the membrane. We’ve combined iDimerize and Tet-On 3G technologies to eliminate these unwanted events. First, use doxycycline (Dox) to optimize the proteins’ expression to physiologically relevant levels. Then induce dimerization by adding the dimerizer ligand to your culture medium.
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