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Figure 2. Four candidates interact with HNF1bbb in GST pull-down assays. Full-length interaction partners with an N-terminal myc-tag were produced in a rabbit reticulocyte system (TNT, Promega) and incubated with the recombinant GST–HNF1bbb fusion protein bound to glutathione sepharose beads. After washing, proteins were recovered and detected by 9E10 mouse anti-myc antibody in Western blots. As controls, GST bound to sepharose or sepharose alone were used.

Image published in: Dudziak K et al. (2008)

Copyright © 2008. This image is reproduced with permission of the publisher and the copyright holder. This is an Open Access article distributed under the terms of the Creative Commons Attribution License.

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