Anti-ACADM Antibody

$99.00$319.00

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

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Rabbit Anti-ACADM Antibody (CSB-PA001126ESR2HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

MCAD Antibody,ACADM Antibody

More alternative names for the antibody
ACAD 1 antibody|ACAD1 antibody|Acadm antibody|ACADM_HUMAN antibody|Acyl coenzyme A dehydrogenase antibody|Acyl coenzyme A dehydrogenase C 4 to C 12 straight chain antibody|FLJ18227 antibody|FLJ93013 antibody|FLJ99884 antibody|MCAD antibody|MCADH antibody|Medium chain acyl CoA dehydrogenase antibody|Medium chain fatty acyl CoA dehydrogenase antibody|Medium chain specific acyl CoA dehydrogenase antibody|Medium chain specific acyl CoA dehydrogenase mitochondrial antibody|Medium-chain specific acyl-CoA dehydrogenase antibody|mitochondrial antibody
Anti-ACADM antibody [3B7BH7] (ab110296)
Close sc-365030|sc-365142|sc-365448|sc-271931|sc-49046|sc-365109|sc-98926|sc-365108|sc-50587|

Recommended applications: ELISA, IHC

Recommended dilution: Recommended dilution:IHC:1:20-1:200

Recommended protocols: check protocols

Name

Anti-ACADM Antibody

Catalogue No.

CSB-PA001126ESR2HU

Reactivity

Human

Immunogen

Recombinant human Medium-chain specific acyl-CoA dehydrogenase, mitochondrial protein (26-421AA)

Host

Rabbit

Applications

ELISA, IHC

Recommended dilution

Recommended dilution:IHC:1:20-1:200

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

46 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:505968( Cow), Entrez Gene:34( Human), Entrez Gene:11364( Mouse), Entrez Gene:24158( Rat), Omim:607008( Human), SwissProt:Q3SZB4( Cow), SwissProt:P11310( Human), SwissProt:P45952( Mouse), SwissProt:P08503( Rat), Unigene:445040( Human), Unigene:10530( Mouse), Unigene:6302( Rat)

Protein function

Acyl-CoA dehydrogenase specific for acyl chain lengths of 4 to 16 that catalyzes the initial step of fatty acid beta-oxidation. Utilizes the electron transfer flavoprotein (ETF) as an electron acceptor to transfer electrons to the main mitochondrial respiratory chain via ETF-ubiquinone oxidoreductase (ETF dehydrogenase). .

Involvement in disease

Acyl-CoA dehydrogenase medium-chain deficiency (ACADMD) [MIM:201450]: An inborn error of mitochondrial fatty acid beta-oxidation which causes fasting hypoglycemia, hepatic dysfunction and encephalopathy, often resulting in death in infancy. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the acyl-CoA dehydrogenase family.

Protein post-translational modifications

Acetylation at Lys-307 and Lys-311 in proximity of the cofactor-binding sites reduces catalytic activity (By similarity). These sites are deacetylated by SIRT3. .

Protein cellular localization

Mitochondrion matrix.

Research area

All research areas>Synthesis and Degradation>MCAD
(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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