ETFDH Antibodies

AND ETFDH ELISA kits, ETFDH Proteins

Many biological assays use antibodies to detect ETFDH, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with ETFDH in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop ETFDH antibodies...

We validate the specificity of these antibodies to ETFDH by testing them on tissues known to express ETFDH positively and negatively. Browse below to find the ETFDH antibody that suites your experiment. We have 1 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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ETFDH Infographic by Boster Bio

All ETFDH Products

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Anti-ETFDH Antibody Picoband®

Western blot analysis of ETFDH using anti-ETFDH antibody (A04340-2)

Flow Cytometry analysis of Jurkat cells using anti-ETFDH antibody (A04340-2)

Human, Mouse, Rat

ELISA, Flow Cytometry, WB

$370
Cat # A04340-2
100 μg/vial

ETFDH Overview

Facts about Electron transfer flavoprotein-ubiquinone oxidoreductase, mitochondrial.

ETFDH 3D structure. Source: alphafold

Electron transfer flavoprotein-ubiquinone oxidoreductase, mitochondrial (ETFDH)

Accepts electrons from ETF and reduces ubiquinone. .

Gene Information

Human
Gene Name:	ETFDH
Uniprot:	Q16134
Entrez:	2110

Family

Belongs to:

ETF-QO/FixC family

Alternative Names

electron-transferring-flavoprotein dehydrogenaseEC 1.5.5.1; ETFQO; ETF-QO; MADD; mitochondrial

Molecular Weight

Mass (kDA):
68.495 kDA

Genomic Context


Human

Location:	4q32.1
Sequence:	4; NC_000004.12 (158672101..158709623)

Subcellular Localizations

Mitochondrion inner membrane.

Diseases

Multiple Acyl Coenzyme A Dehydrogenase Deficiency
Myopathy
Metabolic Diseases
Muscle Weakness
Weakness
Lipoidosis
Inborn Errors Of Metabolism
Encephalopathies
Vomiting
Mitochondrial Diseases

Renal Carnitine Transport Defect
Storage Disease
Triglyceride Storage Disease With Ichthyosis
Ichthyoses
Mitochondrial Myopathies

Pathways

Lipid Storage
Transport
Fatty Acid Oxidation
Localization
Mitochondrial Transport
Electron Transport
Neurogenesis
Oxidative Phosphorylation
Riboflavin Transport

Pathogenesis
Glucose Transport
Glycolysis

PTMs

Oxidation

Phosphorylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/ETFDH

References

PMID: 8306995 by Goodman S.I., et al. Molecular cloning and expression of a cDNA encoding human electron transfer flavoprotein-ubiquinone oxidoreductase.

PMID: 12815589 by Olsen R.K.J., et al. Clear relationship between ETF/ETFDH genotype and phenotype in patients with multiple acyl-CoA dehydrogenation deficiency.