Catalog No.
YHE22101
Expression system
E. coli
Species
Homo sapiens (Human)
Protein length
Ala2-Ile255
Predicted molecular weight
30.02 kDa
Nature
Recombinant
Endotoxin level
Please contact with the lab for this information.
Purity
>90% as determined by SDS-PAGE.
Accession
P38117
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
Beta-ETF, ETFB, Electron transfer flavoprotein subunit beta
Towards a kingdom of reproductive life - the core sperm proteome., PMID:40298292
Performance of electrochemical aptasensor as antigen test in clinical samples for early diagnosis of leptospirosis., PMID:40102450
Lysine 2-hydroxyisobutyrylation of HXK1 alters energy metabolism and KATP channel function in the atrium from patients with atrial fibrillation., PMID:40033384
OXPHOS mediators in acute myeloid leukemia patients: Prognostic biomarkers and therapeutic targets for personalized medicine., PMID:39533394
Transcriptomic Analysis of Cardiac Tissues in a Rodent Model of Coronary Microembolization., PMID:39345897
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
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
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
Electrochemical aptasensor detection of electron transfer flavoprotein subunit beta for leptospirosis diagnosis., PMID:37599631
A Comprehensive LOVD Database for Fatty Acid Oxidation Disorders in Chinese Populations., PMID:40225143
Proteomics reveals specific biological changes induced by the normothermic machine perfusion of donor kidneys with a significant up-regulation of Latexin., PMID:37041202
A novel deleterious ETFA promoter variant causative of multiple acyl-CoA dehydrogenase deficiency., PMID:36579410
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
S1P defects cause a new entity of cataract, alopecia, oral mucosal disorder, and psoriasis-like syndrome., PMID:35362222
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
Quantitative proteomics analysis reveals unique but overlapping protein signatures in HIV infections., PMID:34030014
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
Mitochondrial energetic impairment in a patient with late-onset glutaric acidemia Type 2., PMID:32804429
Integrated analysis of ultra-deep proteomes in cortex, cerebrospinal fluid and serum reveals a mitochondrial signature in Alzheimer's disease., PMID:32711556
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
Hepatic neddylation targets and stabilizes electron transfer flavoproteins to facilitate fatty acid β-oxidation., PMID:31941714
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
A Novel Truncating FLAD1 Variant, Causing Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) in an 8-Year-Old Boy., PMID:30311138
Putative Iron Acquisition Systems in Stenotrophomonas maltophilia., PMID:30115820
Coenzyme Q10 serves to couple mitochondrial oxidative phosphorylation and fatty acid β-oxidation, and attenuates NLRP3 inflammasome activation., PMID:30003820
Role of METTL20 in regulating β-oxidation and heat production in mice under fasting or ketogenic conditions., PMID:29352221
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
Exome array analysis identifies ETFB as a novel susceptibility gene for anthracycline-induced cardiotoxicity in cancer patients., PMID:28913729
Evaluation of the electron transfer flavoprotein as an antibacterial target in Burkholderia cenocepacia., PMID:28817787
Identification of novel biomarker and therapeutic target candidates for diagnosis and treatment of follicular carcinoma., PMID:28709933
ATP5B and ETFB metabolic markers in children with congenital hydronephrosis., PMID:27840937
Functional characterization of electron-transferring flavoprotein and its dehydrogenase required for fungal development and plant infection by the rice blast fungus., PMID:27113712
Significant clinical heterogeneity with similar ETFDH genotype in three Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency., PMID:27000805
New protein-protein interactions of mitochondrial connexin 43 in mouse heart., PMID:26915330
Transcriptional analysis of micronutrient zinc-associated response for enhanced carbohydrate utilization and earlier solventogenesis in Clostridium acetobutylicum., PMID:26586044
An electron transfer flavoprotein is essential for viability and its depletion causes a rod-to-sphere change in Burkholderia cenocepacia., PMID:26253539
For research use only. Not for human or drug use.
