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Fig. S1. Confirmation of selected array clones by RT-PCR analysis. Twenty-five percent of the array clones that resulted upregulated by Gata5 was validated by RT-PCR analysis, reasoning that this was a representative sample size. RT-PCR was performed on cDNA synthesized from ectodermal explants expressing Gata5. ODC was used as loading control and Pdx1 as positive control for Gata5 induction. The primers used for RT-PCR analysis are available at the http://xenopus.rockefeller.edu/.

Image published in: Spagnoli FM and Brivanlou AH (2008)

Copyright © 2008. Image 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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