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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. Zusätzlich bieten wir Ihnen Electron-Transfer-Flavoprotein, beta Polypeptide Antikörper (70) und Electron-Transfer-Flavoprotein, beta Polypeptide Proteine (20) und viele weitere Produktgruppen zu diesem Protein an.
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ETF-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 (zeige AIFM1 ELISA Kits)-Cx43 (zeige GJA1 ELISA Kits), ETFB-Cx43 (zeige GJA1 ELISA Kits) and AIF (zeige AIFM1 ELISA Kits)-ETFB as possible players in the regulation of the mitochondrial redox state.
These results suggested that increasing levels of ATP5B (zeige ATP5B ELISA Kits) 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 (zeige C12orf72 ELISA Kits) is a mitochondrial lysine methyltransferase that targets ETFbeta and modulates its activity.
ETFB knockdown can affect TGF-beta (zeige TGFB1 ELISA Kits)-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 fold, and provided a rationale for the prediction of effects of mutations in ETF.
Tissue samples from 16 unrelated patients with ETF 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