Publishing research using ab11172? Please let us know so that we can cite the reference in this datasheet.

ab11172 has been referenced in 2 publications.

  • Gulhan Ercan-Sencicek A  et al. Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans. Eur J Hum Genet N/A:N/A (2014). Human . PubMed: 24781755
  • Xu Y  et al. Advanced glycation end product (AGE)-receptor for AGE (RAGE) signaling and up-regulation of Egr-1 in hypoxic macrophages. J Biol Chem 285:23233-40 (2010). WB ; Human . PubMed: 20507991

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