Publishing research using ab84816? Please let us know so that we can cite the reference in this datasheet.

ab84816 has been referenced in 4 publications.

  • Nava C  et al. De novo mutations in HCN1 cause early infantile epileptic encephalopathy. Nat Genet 46:640-5 (2014). WB ; Human . PubMed: 24747641
  • Cao-Ehlker X  et al. Up-regulation of hyperpolarization-activated cyclic nucleotide-gated channel 3 (HCN3) by specific interaction with K+ channel tetramerization domain-containing protein 3 (KCTD3). J Biol Chem 288:7580-9 (2013). PubMed: 23382386
  • Fenske S  et al. Sick sinus syndrome in HCN1-deficient mice. Circulation 128:2585-94 (2013). Mouse . PubMed: 24218458
  • Ramakrishnan NA  et al. HCN1 and HCN2 Proteins Are Expressed in Cochlear Hair Cells: HCN1 CAN FORM A TERNARY COMPLEX WITH PROTOCADHERIN 15 CD3 AND F-ACTIN-BINDING FILAMIN A OR CAN INTERACT WITH HCN2. J Biol Chem 287:37628-46 (2012). IHC-FoFr ; Rat . PubMed: 22948144

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