SUOX rabbit pAb

SUOX rabbit pAb

AO-06-ES12883-50

SUOX rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES12883
Product nameSUOX rabbit pAb
ReactivityHuman; Mouse;Rat
ApplicationsWB
Other name
Size50μL
Unit price ($)148
Human gene ID6821
Human Swiss-ProtP51687
SourceRabbit
IsotypeIgG
TargetSUOX
Fields>>Sulfur metabolism;>>Metabolic pathways
Gene nameSUOX
Protein nameSUOX
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID211389
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ8R086
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID81805
Rat gene linkView Rat Gene
Rat Swiss-ProtQ07116
Rat Swiss linkView Rat Swiss-Prot
ImmunogenSynthesized peptide derived from human SUOX AA range: 64-114
SpecificityThis antibody detects endogenous levels of SUOX at Human/Mouse/Rat
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWB 1:500-2000
PurificationThe antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)60kD
Observed band (KD)
BackgroundSulfite 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],
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.,
Subcellular locationMitochondrion intermembrane space .
Expression

Additional Images

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Western blot analysis of lysates from 293T cells, primary antibody was diluted at 1:1000, 4°over night
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: AO-06-ES12883-50
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