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anti-Human ACOX1 Antibodies:
anti-Rat (Rattus) ACOX1 Antibodies:
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Human Polyclonal ACOX1 Primary Antibody for ELISA, WB - ABIN559749
Omi, Nakata, Okamura-Ikeda, Konishi, Taniguchi: Contribution of peroxisome-specific isoform of Lon protease in sorting PTS1 proteins to peroxisomes. in Journal of biochemistry 2008
Show all 2 Pubmed References
Human Polyclonal ACOX1 Primary Antibody for WB - ABIN389100
Strausberg, Feingold, Grouse, Derge, Klausner, Collins, Wagner, Shenmen, Schuler, Altschul, Zeeberg, Buetow, Schaefer, Bhat, Hopkins, Jordan, Moore, Max, Wang, Hsieh, Diatchenko, Marusina, Farmer et al.: Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. ... in Proceedings of the National Academy of Sciences of the United States of America 2002
Show all 5 Pubmed References
Human Polyclonal ACOX1 Primary Antibody for IHC (p) - ABIN389099
Aoyama, Tsushima, Souri, Kamijo, Suzuki, Shimozawa, Orii, Hashimoto: Molecular cloning and functional expression of a human peroxisomal acyl-coenzyme A oxidase. in Biochemical and biophysical research communications 1994
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Human Polyclonal ACOX1 Primary Antibody for ICC, IF - ABIN4277717
Stadler, Rexhepaj, Singan, Murphy, Pepperkok, Uhlén, Simpson, Lundberg: Immunofluorescence and fluorescent-protein tagging show high correlation for protein localization in mammalian cells. in Nature methods 2013
Because patients with AOx deficiency suffer from more severe symptoms than those with X-ALD, accumulation of VLC-PUFA and/or reduction of DHA may be associated with the severity of peroxisomal diseases.
ACOX1 and GNPAT (show GNPAT Antibodies) silencing up-regulated ceramide galactosyltransferase (UGT8 (show UGT8 Antibodies)) mRNA expression, and down-regulated UDP-glucoseceramide glucosyltransferase (UGCG (show UGCG Antibodies)).
Data show that human ACOX1b isoform is more effective than the ACOX1a isoform in reversing the Acox1 null phenotype in the mouse.
Mutational spectrum of peroxisomal acyl-coenzyme A (show SOAT2 Antibodies) oxidase deficiency.
report on two new patients with ACOX1 deficiency and mutational analyses
molecular characterization of the ACOX1 gene; identified one SNP and investigated its association in 7 Bos taurus populations; the A1865C SNP of ACOX1 is significantly associated with ultrasound backfat thickness and ultrasound marbling score in cattle
Our data support a link between oxidative stress and the deficiency of Abcd1 (show ABCD1 Antibodies) or Acox1 peroxisomal proteins.
progressive PPARalpha (show PPARA Antibodies)- and p8-mediated ER stress contribute to the hepatocarcinogenesis in ACOX1(-/-) mice
Loss of Fatty acyl-CoA (show GNPAT Antibodies) oxidase leads to increased amounts of PPARalpha (show PPARA Antibodies), peroxisomal bifunctional enzyme (show EHHADH Antibodies) and thiolase (show HADHB Antibodies) in hepatocellular carcinoma
STAT5A (show STAT5A Antibodies) binds to -1841 to -1825 of the murine AOX promoter.
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.
acyl-Coenzyme A oxidase 1, palmitoyl
, peroxisomal acyl-coenzyme A oxidase 1
, palmitoyl-CoA oxidase
, Acyl-coenzyme A oxidase 1, peroxisomal
, acyl-CoA oxidase 1, palmitoyl
, peroxisomal acyl-coenzyme A oxidase 1-like
, acyl-CoA oxidase, straight-chain
, peroxisomal fatty acyl-CoA oxidase
, straight-chain acyl-CoA oxidase
, palmitoyl acyl-CoA oxidase 1
, peroxisomal fatty acyl-coenzyme A oxidase
, peroxisomal straight-chain Acyl-CoA oxidase
, palmitoyl-CoA oxidase 1