P504S polyclonal antibody; host Rabbit; reactivity Human, Mouse, Rat
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alpha-methylacyl-CoA racemase(AMACR) Homo sapiens This gene encodes a racemase. The encoded enzyme interconverts pristanoyl-CoA and C27-bile acylCoAs between their (R)- and (S)-stereoisomers. The conversion to the (S)-stereoisomers is necessary for degradation of these substrates by peroxisomal beta-oxidation. Encoded proteins from this locus localize to both mitochondria and peroxisomes. Mutations in this gene may be associated with adult-onset sensorimotor neuropathy, pigmentary retinopathy, and adrenomyeloneuropathy due to defects in bile acid synthesis. Alternatively spliced transcript variants have been described. Read-through transcription also exists between this gene and the upstream neighboring C1QTNF3 (C1q and tumor necrosis factor related protein 3) gene. [provided by RefSeq, Mar 2011],
Fully tested in-house by ABMIUM, or supported by an advanced validation report from a partner reviewed by ABMIUM. Highest confidence. Non-conformities fully supported under the ABMIUM Product Promise.
Quality verified. Independent collaborator or expected-performance data available. Product meets ABMIUM quality standards.
Expected to work based on structural and biochemical data. Not yet directly tested by ABMIUM or a collaborator. No non-conformity support for this combination.
Not recommended for this application or species/sample combination. This may indicate either evidence of unsuitability or that the combination has not been tested and therefore cannot currently be recommended.
Evidence status by application and model.
| Species / reactivity | WB | ELISA |
|---|---|---|
| Human,Mouse,Rat |
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AMACR (alpha-methylacyl-CoA racemase; P504S) is a mitochondrial and peroxisomal enzyme that interconverts stereoisomers of alpha-methyl branched acyl-CoA substrates. It is studied in branched-chain fatty-acid oxidation, bile-acid intermediate metabolism and metabolic enzyme expression research.
Biological function: Alpha-methylacyl-CoA racemase converts (2R)-2-methylacyl-CoA esters to the (2S) configuration required for downstream beta-oxidation. Human AMACR acts on substrates derived from branched-chain fatty acids such as pristanic acid and on bile-acid synthesis intermediates, linking peroxisomal and mitochondrial lipid metabolism.
