SKU: WP4373 Categories: ,

SUOX rabbit pAb

Price range: $268.00 through $328.00

SKU: WP4373-100
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Product details

Background:

Sulfite oxidase is a homodimeric protein localized to the intermembrane space of mitochondria. Each subunit contains a heme domain and a molybdopterin-binding domain. The enzyme catalyzes the oxidation of sulfite to sulfate, the final reaction in the oxidative degradation of the sulfur amino acids cysteine and methionine. Sulfite oxidase deficiency results in neurological abnormalities which are often fatal at an early age. Alternative splicing results in multiple transcript variants encoding identical proteins. [provided by RefSeq, Jul 2008],

Specifications

Size50μL/100μL
TargetSUOX
ReactivityHuman, Mouse, Rat
ApplicationsWB
MW(Calculated)60kD
MW(Observed)
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-2000
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration1 mg/ml
ClonalityPolyclonal
Clone Number
ImmunogenSynthesized peptide derived from human SUOX AA range: 64-114
SpecificityThis antibody detects endogenous levels of SUOX at Human/Mouse/Rat
Gene NameSUOX
Protein NameSUOX
Other Name
SpeciesHuman
Gene ID6821
UniprotP51687,
Species.1Mouse
Gene ID.1211389
Uniprot.1Q8R086,
Species.2Rat
Gene ID.281805
Uniprot.2Q07116
Cellular LocalizationMitochondrion intermembrane space .
Tissue Expression
Signaling_pathway
Research Areas>>Sulfur metabolism; / >>Metabolic pathways
FunctionCatalytic activity:Sulfite + O(2) + H(2)O = sulfate + H(2)O(2).,cofactor:Binds 1 protoheme group.,cofactor:Molybdenum (molybdopterin).,Disease:Defects in SUOX are the cause of isolated sulfite oxidase deficiency (ISOD) [MIM:272300]; also known as sulfocysteinuria. ISOD is characterized by neurological abnormalities including multicystic leukoencephalopathy with brain atrophy. Patients often suffer from seizures. Often leads to death at an early age.,pathway:Energy metabolism; sulfur metabolism.,similarity:Contains 1 cytochrome b5 heme-binding domain.,subunit:Homodimer.,
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