MOCOS Polyclonal Antibody | G-AB-08652

MOCOS Polyclonal Antibody | G-AB-08652 | Gentaur Antibodies

Overview: 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.

Category Type: Polyclonal Antibody

Research Areas:

Synonyms: MOCOS, HMCS, MCS, MOS, XAN2

Reactivity: Human

Host: Rabbit

Isotype: IgG

Gene ID: 55034

Accession #:

Clonality:

Immunogen: Recombinant fusion protein of human MOCOS (NP_060417.2) .

Clone #:

Conjugation: Unconjugated

Swissprot: Q96EN8

Santa Cruz:

Calculated MW: 98 kDa

Observed MW: 98 kDa

Concentration: 1 mg/mL

Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3

Purification method: Affinity purification

Application: WB

Dilution: WB 1:500-1:2000

Storage: Store at -20°C. Avoid freeze / thaw cycles.

MOCOS Polyclonal Antibody DataSheet