This is a Validated Antibody Database (VAD) review about human CYP26C1, based on 1 published articles (read how Labome selects the articles), using CYP26C1 antibody in all methods. It is aimed to help Labome visitors find the most suited CYP26C1 antibody. Please note the number of articles fluctuates since newly identified citations are added and citations for discontinued catalog numbers are removed regularly.
CYP26C1 synonym: FFDD4; cytochrome P450 26C1; cytochrome P450, family 26, subfamily C, polypeptide 1

Invitrogen
rabbit polyclonal
  • western blot; human; 1:100; loading ...; fig 3a
In order to examine a three-generation family with SHOX deficiency to identify genes that modulate disease severity, Invitrogen CYP26C1 antibody (Thermo, PA5-15059) was used in western blot on human samples at 1:100 (fig 3a). EMBO Mol Med (2016) ncbi
Articles Reviewed
  1. Montalbano A, Juergensen L, Roeth R, Weiss B, Fukami M, Fricke Otto S, et al. Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency. EMBO Mol Med. 2016;8:1455-1469 pubmed publisher