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ETFB encodes electron-transfer-flavoprotein, beta polypeptide, which shuttles electrons between primary flavoprotein dehydrogenases involved in mitochondrial fatty acid and amino acid catabolism and the membrane-bound electron transfer flavoprotein u. Additionally we are shipping Electron-Transfer-Flavoprotein, beta Polypeptide Kits (30) and Electron-Transfer-Flavoprotein, beta Polypeptide Proteins (20) and many more products for this protein.
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Human Polyclonal ETFB Primary Antibody for ELISA, IHC - ABIN4309650
Ohkuma, Noguchi, Sugie, Malicdan, Fukuda, Shimazu, López, Hirano, Hayashi, Nonaka, Nishino: Clinical and genetic analysis of lipid storage myopathies. in Muscle & nerve 2009
ETF (show TEAD2 Antibodies)-beta has a role as part of the electron transfer flavoprotein complex in the catabolism of leucine and involvement in the chlorophyll degradation pathway activated during dark-induced carbohydrate deprivation.
The results identify new protein-protein interactions between AIF (show AIFM1 Antibodies)-Cx43 (show GJA1 Antibodies), ETFB-Cx43 (show GJA1 Antibodies) and AIF (show AIFM1 Antibodies)-ETFB as possible players in the regulation of the mitochondrial redox state.
These results suggested that increasing levels of ATP5B (show ATP5B Antibodies) and ETFB were associated with worsening renal injury.
the findings of our present study suggest that ETFbeta plays an important role in renal tubular cell apoptosis during the progression of DN.
Electron Transfer Flavoprotein Subunit Beta Is a Candidate Endothelial Cell Autoantigen in Behcet's Disease
Human METTL20 (show C12orf72 Antibodies) is a mitochondrial lysine methyltransferase that targets ETFbeta and modulates its activity.
ETFB knockdown can affect TGF-beta (show TGFB1 Antibodies)-induced tissue remodeling and/or fibrotic processes in vitro.
Point mutations in electron-transfer-flavoprotein beta is associated with destabilized conformations and defective protein:protein interactions leading to mitochondrial dysfunction.
ETFB participates in the mechanoregulation of fibroblast cell number in collagen gel culture.
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).
Tissue samples from 16 unrelated patients with ETF (show TEAD2 Antibodies) deficiency were analysed, two of them harboured mutations in the ETFB gene.
conformational and stability properties of the disease-causing variant ETFbeta-D128N, and our findings on the effect of flavinylation in modulating protein conformational stability and activity.
This gene encodes electron-transfer-flavoprotein, beta polypeptide, which shuttles electrons between primary flavoprotein dehydrogenases involved in mitochondrial fatty acid and amino acid catabolism and the membrane-bound electron transfer flavoprotein ubiquinone oxidoreductase. The gene deficiencies have been implicated in type II glutaricaciduria. Alternatively spliced transcript variants have been found for this gene.
electron transfer flavoprotein subunit beta
, electron transfer flavoprotein beta subunit
, electron transfer flavoprotein beta-subunit
, electron transfer flavoprotein, beta polypeptide
, electron-transferring-flavoprotein, beta polypeptide
, electron transferring flavoprotein, beta polypeptide