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  • SAB4200562 - Monoclonal Anti-AOX1 antibody produced in mouse

SAB4200562 Sigma-Aldrich

Monoclonal Anti-AOX1 antibody produced in mouse

~1.0 mg/mL, clone AO15, purified immunoglobulin

Synonym: Monoclonal Anti-AO, Monoclonal Anti-AOH1, Monoclonal Anti-EC, Monoclonal Anti-aldehyde oxidase 1

  •  NACRES NA.41



Related Categories AO-AQ, Alphabetical Index, Antibodies, Antibodies for Cell Biology, Antibodies for Cell Stress,
conjugate   unconjugated
clone   AO15, monoclonal
biological source   mouse
application(s)   western blot: 1.0-2.0 μg/mL using extracts of HepG2 cells.
species reactivity   human
mol wt   antigen ~148 kDa
form   buffered aqueous solution
shipped in   dry ice
storage temp.   −20°C
antibody form   purified immunoglobulin
isotype   IgG1
Quality Level   200
antibody product type   primary antibodies
concentration   ~1.0 mg/mL
UniProt accession no.   Q06278
Gene Information   human ... AOX1(316)


General description

Monoclonal Anti-AOX1 (mouse IgG1 isotype) is derived from the hybridoma AO15 produced by the fusion of mouse myeloma cells and splenocytes from BALB/c mice immunized with a synthetic peptide. Aldehyde oxidase 1 (AOX1) comprises the 2Fe/2S clusters and two flavin adenine nucleotide (FAD) domain-containing N-terminal domain I and II, respectively. The C-terminal domain encompasses domain III with a substrate-binding site. The gene encoding AOX1 is mapped to human chromosome 2q33.1.


Monoclonal Anti-AOX1 recognizes human AOX1.


synthetic peptide corresponding to an internal sequence of human AOX1. The isotype is determined by ELISA using Mouse Monoclonal Antibody Isotyping Reagents (Sigma ISO-2).


Monoclonal Anti-AOX1 antibody produced in mouse has been used in reverse-phase protein array analysis(5) and immunoblotting.

Physical form

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.

Storage and Stability

For extended storage, freeze at -20 °C in working aliquots. Repeated freezing and thawing,or storage in “frost-free” freezers,isnot recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Working dilution samples should be discarded if not used within 12 hours.


Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

Biochem/physiol Actions

Aldehyde oxidase 1 (AOX1), along with the endoplasmic cytochrome P450 system (CYP450), participates in the drug metabolism and generation of reactive oxygen species. It also has a role in the hepatic phase I metabolism of numerous xenobiotics. Reduced AOX1 protein expression is implicated in chronic pancreatitis, and hepatocellular carcinoma. Furthermore, hypermethylation of the AOX1 promoter region is observed in colon cancer and prostate cancer, making it a potential biomarker for prostate cancer diagnosis. Polymorphism in the AOX1 gene also displays variation in metabolism of the quinoxaline phenoxypropionic acid derivative XK469.

Safety & Documentation

Safety Information

NONH for all modes of transport
Flash Point(F) 
Not applicable
Flash Point(C) 
Not applicable
Protocols & Articles


Antibody Basics

Immunoglobulins (Igs) are produced by B lymphocytes and secreted into plasma. The Ig molecule in monomeric form is a glycoprotein with a molecular weight of approximately 150 kDa that is shaped more ...
Keywords: Affinity chromatography, Centrifugation, Chromatography, Digestions, Direct immunofluorescence, Gene expression, High performance liquid chromatography, Immunofluorescence, Ion Exchange, Microscopy, Precipitation, Purification, Rheumatology, Scanning electron microscopy


Western Blot Protocol | Immunoblotting Protocol

Western Blotting refers to the electrophoretic transfer of proteins from sodium dodecyl sulfate polyacrylamide gels to sheets of PVDF or nitrocellullose membrane, followed by immunodetection of prote...
Keywords: AGE, Buffers, Cell disruption, Detection methods, Detergents, Dialysis, Electroblotting, Electrophoresis, Enzyme activity, Gel electrophoresis, Immunoprecipitation, PAGE, Protein extraction, Purification, Sample preparations, Western blot

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