Alpha-Methylacyl Coenzyme A Racemase (aMACR)
RACE; 2-methylacyl-CoA racemase
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AMACR deficiency has recently been discovered. The first documented case was in 2006. It is in a class of disorders called peroxisome biogenesis disorders (PBD) although it is quite different than other peroxisomal disorders and does not share classic Refsum disorder symptoms. It causes an accumulation of pristanic acid, DHCA and EHCA and to a lesser extent VLCFA and phytanic acid. "His condition would have been missed if they hadn't measured the pristanic acid concentration."
It can cause mental impairment,confusion, learning difficulties and liver damage. It can be treated by dietary elimination of pristanic and phytanic acid from meats such as beef, lamb, chicken, and dairy products, however compliance to the diet is low due to dietary habits, and loss of weight.
Organism species: Homo sapiens (Human)
- Recombinant protein RPJ647Hu01 Recombinant Alpha-Methylacyl Coenzyme A Racemase (aMACR) In Stock
- Monoclonal antibody MAJ647Hu21 Monoclonal Antibody to Alpha-Methylacyl Coenzyme A Racemase (aMACR) In Stock
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- Sandwich ELISA SEJ647Hu ELISA Kit for Alpha-Methylacyl Coenzyme A Racemase (aMACR) In Stock
Organism species: Mus musculus (Mouse)
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Organism species: Rattus norvegicus (Rat)
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