Key features and details
- Rabbit polyclonal to ACADM/MCAD
- Suitable for: WB
- Reacts with: Mouse, Sheep, Human, Pig
- Isotype: IgG
Product nameAnti-ACADM/MCAD antibody
See all ACADM/MCAD primary antibodies
DescriptionRabbit polyclonal to ACADM/MCAD
Tested applicationsSuitable for: WBmore details
Species reactivityReacts with: Mouse, Sheep, Human, Pig
Recombinant full length protein corresponding to Human ACADM/MCAD.
Previously labelled as ACADM.
Storage instructionsShipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Storage bufferpH: 7.40
Preservative: 0.02% Sodium azide
Constituents: Tris buffered saline, 50% Glycerol, 0.1% BSA
Concentration information loading...
PurityProtein A purified
- Pathways and Processes
- Metabolic signaling pathways
- Lipid and lipoprotein metabolism
- Lipid metabolism
Our Abpromise guarantee covers the use of ab23675 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|WB||1/200. Predicted molecular weight: 43 kDa.|
FunctionThis enzyme is specific for acyl chain lengths of 4 to 16.
PathwayLipid metabolism; mitochondrial fatty acid beta-oxidation.
Involvement in diseaseDefects in ACADM are the cause of acyl-CoA dehydrogenase medium-chain deficiency (ACADMD) [MIM:201450]. It is an autosomal recessive disease which causes fasting hypoglycemia, hepatic dysfunction, and encephalopathy, often resulting in death in infancy.
Sequence similaritiesBelongs to the acyl-CoA dehydrogenase family.
Cellular localizationMitochondrion matrix.
- Information by UniProt
- ACAD 1 antibody
- ACAD1 antibody
- Acadm antibody
ab23675 has been referenced in 1 publication.
- Bartha JL et al. Tissue specific expression of human fatty acid oxidation enzyme genes in late pregnancy. Lipids Health Dis 15:200 (2016). WB ; Human . PubMed: 27871288