Ethylmalonic encephalopathy 1
This gene encodes a member of the metallo beta-lactamase family of iron-containing proteins involved in the mitochondrial sulfide oxidation pathway. The encoded protein catalyzes the oxidation of a persulfide substrate to sulfite. Certain mutations in this gene cause ethylmalonic encephalopathy, an infantile metabolic disorder affecting the brain, gastrointestinal tract and peripheral vessels. Alternative splicing results in multiple transcript variants encoding different isoforms.
Mouse Anti-ETHE1 Antibody (CBMOAB-00056HCB) (CAT#: CBMOAB-00056HCB)
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- Host species: Mouse
- Species Reactivity: C. elegans (Caenorhabditis elegans), Cattle (Bos taurus), Chimpanzee (Pan troglodytes), Frog (Xenopus laevis), Marmoset, Rat (Rattus norvegicus), Zebrafish (Danio rerio)
- Application: WB, ELISA
- Protein: Submitted name: Lactamase_B domain-containing protein
- Size: 0.5mg, 1mg, 200µg
- Conjugate: AP, APC, Biotin, Consult us more, Cy3, Cy5, Cy5.5, Cy7, FITC, HRP, NONE, PE, PerCP
- Alternative Names: Protein ETHE-1, ethe-1
For Research Use Only | Not For Clinical Use.
