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Recombinant Human Sulfite oxidase, mitochondrial (SUOX)

The region for expressing recombinant Human SUOX contains amino acids 80-545. This SUOX protein is expected to have a theoretical molecular weight of 67.6 kDa. The SUOX protein was expressed in e.coli. The SUOX coding gene included the N-terminal 6xHis-SUMO tag, which simplifies the detection and purification processes of the recombinant SUOX protein in following stages of expression and purification.Sulfite oxidase, mitochondrial (SUOX) is a crucial enzyme involved in the oxidation of sulfite to sulfate in the mitochondria. This process is vital for the metabolism of sulfur-containing amino acids, such as cysteine and methionine. SUOX plays a pivotal role in maintaining sulfur homeostasis and preventing the accumulation of toxic sulfite levels in the body. Additionally, SUOX is essential for the proper functioning of the molybdenum cofactor (Moco), a prosthetic group required for the enzyme's activity. Mutations in the SUOX gene can lead to a rare inherited disorder known as isolated sulfite oxidase deficiency, characterized by neurological abnormalities and other health complications. Research on SUOX contributes to a better understanding of sulfur metabolism, redox balance, and the molecular basis of genetic disorders related to sulfite oxidase deficiency.

ACP04759

The region for expressing recombinant Human SUOX contains amino acids 80-545. This SUOX protein is expected to have a theoretical molecular weight of 67.6 kDa. The SUOX protein was expressed in e.coli. The SUOX coding gene included the N-terminal 6xHis-SUMO tag, which simplifies the detection and purification processes of the recombinant SUOX protein in following stages of expression and purification.Sulfite oxidase, mitochondrial (SUOX) is a crucial enzyme involved in the oxidation of sulfite to sulfate in the mitochondria. This process is vital for the metabolism of sulfur-containing amino acids, such as cysteine and methionine. SUOX plays a pivotal role in maintaining sulfur homeostasis and preventing the accumulation of toxic sulfite levels in the body. Additionally, SUOX is essential for the proper functioning of the molybdenum cofactor (Moco), a prosthetic group required for the enzyme’s activity. Mutations in the SUOX gene can lead to a rare inherited disorder known as isolated sulfite oxidase deficiency, characterized by neurological abnormalities and other health complications. Research on SUOX contributes to a better understanding of sulfur metabolism, redox balance, and the molecular basis of genetic disorders related to sulfite oxidase deficiency.

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Specifications


Cat.No ACP04759 Target NameSUOX
Target SynonymsEC 1.8.3.1; mitochondrial; Sulfite oxidase; Sulfite oxidase mitochondrial ; Sulfite oxidase; mitochondrial precursor; Suox; SUOX_HUMANFormLiquid or Lyophilized powder
Expression SystemE.coliExpression Range80-545aa
Mol Weight67.6kDaProtein LengthFull Length of Mature Protein
PurityGreater than 90% as determined by SDS-PAGE.Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDP51687
Background Information
  • Uniprot Id

    P51687

  • Target Species

    Human

  • Target Name

    SUOX

  • Target Full Name

    Sulfite oxidase, mitochondrial

  • Target Involvement

    Isolated sulfite oxidase deficiency (ISOD)

  • Target Subcellular Location

    Mitochondrion intermembrane space.

  • Target Research Area

    Metabolism

  • Target Synonyms

    EC 1.8.3.1; mitochondrial; Sulfite oxidase; Sulfite oxidase mitochondrial ; Sulfite oxidase; mitochondrial precursor; Suox; SUOX_HUMAN

  • Target 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.

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