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The antibody against MOCOS was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 649-888 of human MOCOS (NP_060417.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.
The antibody against MOCOS was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 649-888 of human MOCOS (NP_060417.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.
| Cat.No | ADA-00657A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | MOCOS |
| Target Synonyms | MCS; MOS; HMCS; MOCOS | Form | Liquid |
| Species Reactivity | Human | Isotype | IgG |
| Storage Buffer | 50% Glycerol, PBS with 0.01% thimerosal, pH7.3. | Purification Method | Affinity purification |
| Positive Samples | HepG2 | Application | ELISA, WB |
| Immunogen Description | Recombinant fusion protein containing a sequence corresponding to amino acids 649-888 of human MOCOS (NP_060417.2). | Target Species | Human |
|---|---|---|---|
| Uniprot ID | Q96EN8 | Immunogen Sequence |
Uniprot Id
Q96EN8
Target Species
Human
Target Name
MOCOS
Target Full Name
Molybdenum cofactor sulfurase
Target Function
Sulfurates the molybdenum cofactor. Sulfation of molybdenum is essential for xanthine dehydrogenase (XDH) and aldehyde oxidase (ADO) enzymes in which molybdenum cofactor is liganded by 1 oxygen and 1 sulfur atom in active form. In vitro, the C-terminal domain is able to reduce N-hydroxylated prodrugs, such as benzamidoxime.
Target Involvement
Xanthinuria 2 (XAN2)
Target Protein Families
Class-V pyridoxal-phosphate-dependent aminotransferase family, MOCOS subfamily
Target Synonyms
MOCOS; Molybdenum cofactor sulfurase; MCS; MOS; MoCo sulfurase; hMCS; EC 2.8.1.9; Molybdenum cofactor sulfurtransferase
Target Background
This gene encodes an enzyme that sulfurates the molybdenum cofactor which is required for activation of the xanthine dehydrogenase (XDH) and aldehyde oxidase (AO) enzymes. XDH catalyzes the conversion of hypoxanthine to uric acid via xanthine, as well as the conversion of allopurinol to oxypurinol, and pyrazinamide to 5-hydroxy pyrazinamide. Mutations in this gene cause the metabolic disorder classical xanthinuria type II which is characterized by the loss of XDH/XO and AO enzyme activity, decreased levels of uric acid in the urine, increased levels of xanthine and hypoxanthine in the serum and urine, formation of xanthine stones in the urinary tract, and myositis due to tissue deposition of xanthine.
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