Catalog No.
YMD01401
Expression system
E. coli
Species
Mus musculus (Mouse)
Protein length
Gln20-Lys333
Predicted molecular weight
34.04 kDa
Nature
Recombinant
Endotoxin level
Please contact with the lab for this information.
Purity
>90% as determined by SDS-PAGE.
Accession
Q99LC5
Applications
ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Form
Lyophilized
Storage buffer
Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.
Reconstitution
Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.
Shipping
In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.
Stability and Storage
Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
Alternative Names
Electron transfer flavoprotein subunit alpha, mitochondrial, Alpha-ETF, Etfa
Genetic insights into the role of mitochondria-related genes in mental disorders: An integrative multi-omics analysis., PMID:40180044
Proteomics reveals genetic mechanisms of cold resistance in Hezuo pig liver tissue., PMID:40064419
Tryptophan metabolism-related gene CYP1B1 serves as a shared biomarker for both Parkinson's disease and insomnia., PMID:39779759
Hepatocyte-derived Igκ promotes HCC progression by stabilizing electron transfer flavoprotein subunit α to facilitate fatty acid β-oxidation., PMID:39380077
MADD-like pattern of acylcarnitines associated with sertraline use., PMID:39318848
Deep Intronic ETFDH Variants Represent a Recurrent Pathogenic Event in Multiple Acyl-CoA Dehydrogenase Deficiency., PMID:39273584
Pomalidomide sensitizes lung cancer cells to TRAIL/CDDP-induced apoptosis via directly targeting electron transfer flavoprotein alpha subunit., PMID:39265523
A compound heterozygote case of glutaric aciduria type II in a patient carrying a novel candidate variant in ETFDH gene: A case report and literature review on compound heterozygote cases., PMID:38967380
Molecular genetic analysis of candidate genes for glutaric aciduria type II in a cohort of patients from Queensland, Australia., PMID:38941880
Platelet Microparticle-Derived MiR-320b Inhibits Hypertension with Atherosclerosis Development by Targeting ETFA., PMID:38556340
Mechanism of Cr(VI) bioreduction by Clostridium sp. LQ25 under Fe(III) reducing conditions., PMID:38171403
Characterization of the Membrane-Associated Electron-Bifurcating Flavoenzyme EtfABCX from the Hyperthermophilic Bacterium Thermotoga maritima., PMID:38061393
A Comprehensive LOVD Database for Fatty Acid Oxidation Disorders in Chinese Populations., PMID:40225143
Can pioglitazone be used for optimization of nutrition in critical illness? A systematic review., PMID:36700419
A novel deleterious ETFA promoter variant causative of multiple acyl-CoA dehydrogenase deficiency., PMID:36579410
Australian genome-wide association study confirms higher female risk for adult glioma associated with variants in the region of CCDC26., PMID:36541697
orsai, the Drosophila homolog of human ETFRF1, links lipid catabolism to growth control., PMID:36266680
A fatal case of neonatal onset multiple acyl-CoA dehydrogenase deficiency caused by novel mutation of ETFDH gene: case report., PMID:36064718
Structure-based electron-confurcation mechanism of the Ldh-EtfAB complex., PMID:35748623
Characterization of 31 Patients with Riboflavin-Responsive Multiple acyl-CoA Dehydrogenase Deficiency., PMID:35734957
S1P defects cause a new entity of cataract, alopecia, oral mucosal disorder, and psoriasis-like syndrome., PMID:35362222
Electron Transfer Flavoprotein (ETF) α Controls Blood Vessel Development by Regulating Endothelial Mitochondrial Bioenergetics and Oxygen Consumption., PMID:35313640
Multi-omics reveals mitochondrial metabolism proteins susceptible for drug discovery in AML., PMID:35177813
Multiple acyl-CoA dehydrogenase deficiency kills Mycobacterium tuberculosis in vitro and during infection., PMID:34782606
Hypoketotic hypoglycemia without neuromuscular complications in patients with SLC25A32 deficiency., PMID:34764427
Clinical, Biochemical, and Genetic Heterogeneity in Glutaric Aciduria Type II Patients., PMID:34573316
NBPF4 mitigates progression in colorectal cancer through the regulation of EZH2-associated ETFA., PMID:34405537
Riboflavin in Neurological Diseases: A Narrative Review., PMID:33886098
Electron transfer flavoprotein and its role in mitochondrial energy metabolism in health and disease., PMID:33450351
Disorders of flavin adenine dinucleotide metabolism: MADD and related deficiencies., PMID:33279678
Anti-Aβ Antibody Aducanumab Regulates the Proteome of Senile Plaques and Closely Surrounding Tissue in a Transgenic Mouse Model of Alzheimer's Disease., PMID:33252074
Pioglitazone corrects dysregulation of skeletal muscle mitochondrial proteins involved in ATP synthesis in type 2 diabetes., PMID:33137378
Mitochondrial energetic impairment in a patient with late-onset glutaric acidemia Type 2., PMID:32804429
Angiogenesis Analyzer for ImageJ - A comparative morphometric analysis of "Endothelial Tube Formation Assay" and "Fibrin Bead Assay"., PMID:32665552
A novel electron transfer flavoprotein dehydrogenase (ETFDH) gene mutation identified in a newborn with glutaric acidemia type II: a case report of a Chinese family., PMID:32393189
A case report of a mild form of multiple acyl-CoA dehydrogenase deficiency due to compound heterozygous mutations in the ETFA gene., PMID:31996215
Hepatic neddylation targets and stabilizes electron transfer flavoproteins to facilitate fatty acid β-oxidation., PMID:31941714
[Tandem mass spectrometry analysis and genetic diagnosis of neonates with fatty acid oxidation disorders in central and northern regions of Guangxi]., PMID:31703127
Molecular and Clinical Investigations on Portuguese Patients with Multiple acyl-CoA Dehydrogenase Deficiency., PMID:31418342
FLAD1-associated multiple acyl-CoA dehydrogenase deficiency identified by newborn screening., PMID:31392824
Determinants of Riboflavin Responsiveness in Multiple Acyl-CoA Dehydrogenase Deficiency., PMID:31331668
Flavin adenine dinucleotide synthase deficiency due to FLAD1 mutation presenting as multiple acyl-CoA dehydrogenation deficiency-like disease: A case report., PMID:30982706
Hyperammonemia after capecitabine associated with occult impairment of the urea cycle., PMID:30977266
Comparative Analysis of Mitochondrial Proteome Reveals the Mechanism of Enhanced Ram Sperm Motility Induced by Carbon Ion Radiation After In Vitro Liquid Storage., PMID:30733653
The catalytic mechanism of electron-bifurcating electron transfer flavoproteins (ETFs) involves an intermediary complex with NAD<sup/>., PMID:30567738
A Novel Truncating FLAD1 Variant, Causing Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) in an 8-Year-Old Boy., PMID:30311138
Coenzyme Q10 serves to couple mitochondrial oxidative phosphorylation and fatty acid β-oxidation, and attenuates NLRP3 inflammasome activation., PMID:30003820
Oxidation of the FAD cofactor to the 8-formyl-derivative in human electron-transferring flavoprotein., PMID:29301933
The semiquinone swing in the bifurcating electron transferring flavoprotein/butyryl-CoA dehydrogenase complex from Clostridium difficile., PMID:29146947
For research use only. Not for human or drug use.
