Loading...
Products:Signal Transduction >> Metabolism >> Energy Metabolism
If your product does not perform as described on this datasheet, we will refund or replace your product...
Read our guarantee »Anti-Xanthine Oxidase antibody (HRP)
See all Xanthine Oxidase products (6) ...
Rabbit polyclonal to Xanthine Oxidase (HRP)
HRP
WB, ELISA, Immunomicroscopy, Dot Blotmore details
Reacts with
Mouse, Cow
Xanthine Oxidase (from Bovine Buttermilk)
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze / thaw cycles.
Preservative: 0.01% Gentamicin Sulfate
Constituents: 10mg/ml BSA, 0.15M Sodium chloride, 0.02M Potassium phosphate. pH 7.2
Concentration information loading...
IgG fraction
Purified from monospecific antiserum by a multi-step process which includes delipidation, salt fractionation and ion exchange chromatography.
Polyclonal
IgG
Metabolism >> Types of disease >> Cancer
Metabolism >> Pathways and Processes >> Metabolic signaling pathways >> Energy transfer pathways >> Energy Metabolism
Signal Transduction >> Metabolism >> Energy Metabolism
Our Abpromise guarantee covers the use of ab34617 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Dot: Use at an assay dependent dilution.
ELISA: 1/35,000 - 1/175,000. Assayed against 1.0 ug of Xanthine Oxidase (Bovine
Buttermilk) in a standard capture ELISA using ABTS (2,2'-azino-bis-[3-ethylbenthiazoline-6-sulfonic acid]) as a substrate for 30 minutes at room temperature.
IM: Use at an assay dependent dilution.
WB: Use at an assay dependent dilution. Predicted molecular weight: 146 kDa.
Not yet tested in other applications.
Optimal dilutions/concentrations should be determined by the end user.
Key enzyme in purine degradation. Catalyzes the oxidation of hypoxanthine to xanthine. Catalyzes the oxidation of xanthine to uric acid. Contributes to the generation of reactive oxygen species. Has also low oxidase activity towards aldehydes (in vitro).
Detected in milk (at protein level).
Defects in XDH are the cause of xanthinuria type 1 (XU1) [MIM:278300]. Xanthinuria is characterized by excretion of very large amounts of xanthine in the urine and a tendency to form xanthine stones. Uric acid is strikingly diminished in serum and urine. XU1 is due to isolated xanthine dehydrogenase. XU1 patients can metabolize allopurinol.
Belongs to the xanthine dehydrogenase family.
Contains 1 2Fe-2S ferredoxin-type domain.
Contains 1 FAD-binding PCMH-type domain.
Subject to partial proteolysis; this alters the enzyme from the dehydrogenase form (D) to the oxidase form (O).
Contains sulfhydryl groups that are easily oxidized (in vitro); this alters the enzyme from the dehydrogenase form (D) to the oxidase form (O).
Cytoplasm. Peroxisome. Secreted.
Target information above from: UniProt accessionP47989
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
ab34617 has not yet been referenced specifically in any publications.
Publishing research using ab34617? Please let us know so that we can cite the reference in this datasheet
Concentration of lot no. is
Concentration not available for this lot.
Find concentration of your lot:
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
Call 01223 696 000 or contact us
