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ETFA participates in catalyzing the initial step of the mitochondrial fatty acid beta-oxidation. Additionally we are shipping Electron-Transfer-Flavoprotein, alpha Polypeptide Proteins (11) and Electron-Transfer-Flavoprotein, alpha Polypeptide Kits (4) and many more products for this protein.
Showing 10 out of 111 products:
Human Polyclonal ETFA Primary Antibody for EIA, FACS - ABIN952127
Chiong, Sim, Carpenter, Rhead, Ho, Olsen, Christodoulou: Transient multiple acyl-CoA dehydrogenation deficiency in a newborn female caused by maternal riboflavin deficiency. in Molecular genetics and metabolism 2007
Show all 3 references for ABIN952127
Human Polyclonal ETFA Primary Antibody for EIA, WB - ABIN569619
Ohkuma, Noguchi, Sugie, Malicdan, Fukuda, Shimazu, López, Hirano, Hayashi, Nonaka, Nishino: Clinical and genetic analysis of lipid storage myopathies. in Muscle & nerve 2009
the mechanism of tert (show TERT Antibodies)-butyl hydroperoxide-induced an apoptosis cascade and endoplasmic reticulum stress in hepatocyte cells by up-regulation of ETFA, providing a new mechanism for liver injury.
These results are consistent with the electron transfer flavoprotein alpha II (show GSTA3 Antibodies) domain adopting orientations in solution that deviate from the crystal structure of free ETF (show TEAD2 Antibodies) towards the active, substrate-bound orientation.
Data established structural hotspots within the ETF (show TEAD2 Antibodies) fold, and provided a rationale for the prediction of effects of mutations in ETF (show TEAD2 Antibodies).
These studies indicate that a series of conformational changes occur during the assembly of the TMADH.ETF electron transfer complex and that the kinetics of assembly observed with mutant TMADH or ETF (show TEAD2 Antibodies) complexes are much slower
Tissue samples from 16 unrelated patients with ETF (show TEAD2 Antibodies) deficiency were analysed and the majority of the patients had mutations in the ETFA gene.
No mutations in electron-transfer-flavoprotein (show ETFB Antibodies) but maternal riboflavin deficiency led to multiple acyl-CoA (show GNPAT Antibodies) dehydrogenation deficiency
ETFA participates in catalyzing the initial step of the mitochondrial fatty acid beta-oxidation. It shuttles electrons between primary flavoprotein dehydrogenases and the membrane-bound electron transfer flavoprotein ubiquinone oxidoreductase. Defects in electron-transfer-flavoprotein have been implicated in type II glutaricaciduria in which multiple acyl-CoA dehydrogenase deficiencies result in large excretion of glutaric, lactic, ethylmalonic, butyric, isobutyric, 2-methyl-butyric, and isovaleric acids. Two transcript variants encoding different isoforms have been found for this gene.
electron transfer flavoprotein, alpha polypeptide
, electron-transfer-flavoprotein, alpha polypeptide (glutaric aciduria II)
, electron transfer flavoprotein subunit alpha, mitochondrial
, electron-transfer-flavoprotein, alpha polypeptide
, electron-transfer-flavoprotein alpha polypeptide
, mitochondrial electron transfer flavoprotein subunit alpha
, electron transferring flavoprotein, alpha polypeptide
, electron transfer flavoprotein alpha-subunit
, glutaric aciduria II
, electron transfer flavoprotein alpha-subunit, mitochondrial
, electron transfer flavoprotein alpha subunit