The protein encoded by this gene is the first enzyme of the fatty acid beta-oxidation pathway, which catalyzes the desaturation of acyl-CoAs to 2-trans-enoyl-CoAs. It donates electrons directly to molecular oxygen, thereby producing hydrogen peroxide. Defects in this gene result in pseudoneonatal adrenoleukodystrophy, a disease that is characterized by accumulation of very long chain fatty acids. Alternatively spliced transcript variants encoding different isoforms have been identified.
WB 1:500 - 1:2000
IHC 1:100 - 1:200
IF 1:50 - 1:200
Recombinant fusion protein containing a sequence corresponding to amino acids 1-270 of human ACOX1 (NP_004026.2).
Western blot analysis of extracts of various cell lines, using ACOX1 antibody (144-08091) at 1:1000 dilution.
Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.
Lysates/proteins: 25ug per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit.
Exposure time: 30s.
Immunohistochemistry of paraffin-embedded mouse brain using ACOX1 antibody (144-08091) at dilution of 1:100 (40x lens).
Immunofluorescence analysis of U2OS cells using ACOX1 antibody (144-08091) at dilution of 1:100. Blue: DAPI for nuclear staining.
12 months from the date of shipment when stored properly.