Background:  Sulfite oxidase (SO), a homodimeric protein that localizes to the intermembrane space of mitochondria, catalyzes the oxidation of sulfite to sulfate, the terminal reaction in the oxidative degradation of the sulfur amino acids cysteine and methionine. Genetic deficiency of SO contributes to neurological abnormalities and often leads to death at an early age. Mutation of Arginine 160 in humans decreases the intramolecular electron transfer (IET) rate, which contributes to the fatality of this genetic disorder. Also, the tyrosine 343 residue in humans plays an important role in both substrate binding and oxidation of sulfite by SO. The human SO gene maps to chromosome 12, and shows high expression in liver, kidney, skeletal muscle, heart, placenta and brain.

Description: Rabbit polyclonal to Sulfite oxidase

Immunogen: KLH conjugated synthetic peptide derived from Sulfite oxidase

Specificity:  ·Reacts with Human, Mouse and Rat.

·Isotype: IgG

Application:  ·Western blotting: 1/100-500. Predicted Mol wt: 60 kDa;

·Immunohistochemistry (Paraffin/frozen tissue section): 1/50-200;

·Immunocytochemistry/Immunofluorescence: 1/100;

·Immunoprecipitation: 1/50;

·ELISA: 1/500;

·Optimal working dilutions must be determined by the end user.