Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
ETHE1 encodes a sulfur dioxygenase that localizes within the mitochondrial matrix. Additionally we are shipping ETHE1 Proteins (13) and ETHE1 Kits (4) and many more products for this protein.
Showing 10 out of 47 products:
Human Polyclonal ETHE1 Primary Antibody for EIA, WB - ABIN452982
Tiranti, Viscomi, Hildebrandt, Di Meo, Mineri, Tiveron, Levitt, Prelle, Fagiolari, Rimoldi, Zeviani: Loss of ETHE1, a mitochondrial dioxygenase, causes fatal sulfide toxicity in ethylmalonic encephalopathy. in Nature medicine 2009
Show all 2 references for ABIN452982
Human Polyclonal ETHE1 Primary Antibody for EIA, WB - ABIN452981
Mineri, Rimoldi, Burlina, Koskull, Perletti, Heese, von Döbeln, Mereghetti, Di Meo, Invernizzi, Zeviani, Uziel, Tiranti: Identification of new mutations in the ETHE1 gene in a cohort of 14 patients presenting with ethylmalonic encephalopathy. in Journal of medical genetics 2008
Show all 2 references for ABIN452981
ETHE1 R163W/R163Q mutations are associated with Ethylmalonic encephalopathy.
Case Report: metabolic disturbances in 15-month-old male presenting with typical ethylmalonic encephalopathy associated with a homozygous ETHE1 mutation.
T152I mutation of ETHE1 results in a 3-fold lower activity.
role of the ETHE1 gene product in mitochondrial homeostasis and energy metabolism
Mutations of ETHE1 were detected in all the typical ethylmalonic encephalopathy patients analysed, but no ETHE1 mutations were identified in patients presenting with early onset progressive encephalopathy with ethylmalonic aciduria.
structural comparison of human ETHE1 and At1g53580 from Arabidopsis thaliana
14 patients with EE were investigated for mutations in the ETHE1 gene. Of the 14 patients, 5 were found to carry novel mutations.
ETHE1 is a mitochondrial sulfur dioxygenase involved in catabolism of sulfide (show SQRDL Antibodies) that accumulates to toxic levels in ethylmalonic encephalopathy.
Ethe1 deficiency disrupts post translational amino acid modification and mitochondrial metabolic systems.
This gene encodes a sulfur dioxygenase that localizes within the mitochondrial matrix. The enzyme functions in sulfide catabolism. Mutations in this gene result in ethylmalonic encephalopathy.
protein ETHE1, mitochondrial
, ethylmalonic encephalopathy 1
, ethylmalonic encephalopathy protein 1
, hepatoma subtracted clone one protein
, persulfide dioxygenase ETHE1, mitochondrial
, sulfur dioxygenase ETHE1
, ethylmalonic encephalopathy protein 1 homolog