Anti-ETFDH Antibody

$99.00$319.00

Reactivity: Human,Mouse
Applications: ELISA,WB,IHC
Conjugation: Various
Supplier: CUSABIO BIOTECH CO.

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Rabbit Anti-ETFDH Antibody (CSB-PA619056ESR2HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

Electron transfer flavoprotein-ubiquinone oxidoreductase Antibody,mitochondrial Antibody,ETF-QO Antibody,ETF-ubiquinone oxidoreductase Antibody,Electron-transferring-flavoprotein dehydrogenase Antibody,ETF dehydrogenase Antibody,ETFDH Antibody

More alternative names for the antibody
Electron transfer flavoprotein ubiquinone oxidoreductase antibody|Electron transfer flavoprotein-ubiquinone oxidoreductase antibody|electron transferring flavoprotein dehydrogenase antibody|Electron-transferring-flavoprotein dehydrogenase antibody|ETF dehydrogenase antibody|ETF QO antibody|ETF ubiquinone oxidoreductase antibody|ETF-QO antibody|ETF-ubiquinone oxidoreductase antibody|ETFD_HUMAN antibody|Etfdh antibody|mitochondrial antibody
Anti-ETFDH antibody [3D1AC4AF3] (ab131376)
Close sc-242642|

Recommended applications: ELISA, WB, IHC

Recommended dilution: User optimized

Recommended protocols: check protocols

Name

Anti-ETFDH Antibody

Catalogue No.

CSB-PA619056ESR2HU

Reactivity

Human, Mouse

Immunogen

Recombinant human Electron transfer flavoprotein-ubiquinone oxidoreductase, mitochondrial protein (318-617AA)

Host

Rabbit

Applications

ELISA, WB, IHC

Recommended dilution

User optimized

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

68 kDa

Purification

Antigen Affinity Purified

Storage

Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.

Database links

Entrez Gene:768074( Cow), Entrez Gene:2110( Human), Entrez Gene:66841( Mouse), Entrez Gene:295143( Rat), Omim:231675( Human), SwissProt:Q2KIG0( Cow), SwissProt:Q16134( Human), SwissProt:Q921G7( Mouse), SwissProt:Q6UPE1( Rat), Unigene:155729( Human), Unigene:28336( Mouse), Unigene:37277( Rat)

Protein function

Accepts electrons from ETF and reduces ubiquinone.

Involvement in disease

Glutaric aciduria 2C (GA2C) [MIM:231680]: An autosomal recessively inherited disorder of fatty acid, amino acid, and choline metabolism. It is characterized by multiple acyl-CoA dehydrogenase deficiencies resulting in large excretion not only of glutaric acid, but also of lactic, ethylmalonic, butyric, isobutyric, 2-methyl-butyric, and isovaleric acids. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the ETF-QO/FixC family.

Protein cellular localization

Mitochondrion inner membrane.

Research area

All research areas>Synthesis and Degradation>ETFDH
(View all antibody categories related to Synthesis and Degradation)

Note

AntibodyPlus provides antibody trial sample for your own antibody validation and collects antibody reviews.

Supplier

CUSABIO BIOTECH CO.

Product type

Primary antibody

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