ACAD-9 rabbit pAb
This gene encodes a member of the acyl-CoA dehydrogenase family. Members of this family of proteins localize to the mitochondria and catalyze the rate-limiting step in the beta-oxidation of fatty acyl-CoA. The encoded protein is specifically active toward palmitoyl-CoA and long-chain unsaturated substrates. Mutations in this gene cause acyl-CoA dehydrogenase family member type 9 deficiency. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010],
Product Specifications
Background
UniProt
Q9H845
Swiss Prot
Q9H845
Reactivity
Human; Mouse; Rat
Immunogen
Synthesized peptide derived from ACAD-9 . at AA range: 530-610
Clonality
Polyclonal
Source
Rabbit
Applications
IHC; IF; ELISA
Concentration
1 mg/ml
Dilution
Immunohistochemistry: 1/100 - 1/300. ELISA: 1/20000. Not yet tested in other applications.
Storage Conditions
-20°C/1 year
Fragment
IgG
Subcellular Location
Mitochondrion inner membrane ; Peripheral membrane protein ; Matrix side . Essentially associated with membranes. .
Other Product Names
ACAD9; Acyl-CoA dehydrogenase family member 9; mitochondrial; ACAD-9
Gene ID (Human)
28976
Available Sizes
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