Human Alpha-Methylacyl Coenzyme A Racemase (aMACR) ELISA Kit | aMACR elisa kit
Human Alpha-Methylacyl Coenzyme A Racemase (aMACR) ELISA Kit
No significant cross-reactivity or interference between Alpha-Methylacyl Coenzyme A Racemase (aMACR) and analogues was observed.
To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.
NCBI and Uniprot Product Information
NCBI Description
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]
Uniprot Description
AMACR: Racemization of 2-methyl-branched fatty acid CoA esters. Responsible for the conversion of pristanoyl-CoA and C27-bile acyl-CoAs to their (S)-stereoisomers. Belongs to the CaiB/BaiF CoA-transferase family. 3 isoforms of the human protein are produced by alternative splicing.
Protein type: Mitochondrial; EC 5.1.99.4; Lipid Metabolism - primary bile acid biosynthesis; Isomerase
Chromosomal Location of Human Ortholog: 5p13
Cellular Component: peroxisomal matrix; mitochondrion; cytoplasm; peroxisome
Molecular Function: receptor binding; alpha-methylacyl-CoA racemase activity
Biological Process: bile acid biosynthetic process; fatty acid beta-oxidation using acyl-CoA oxidase; bile acid metabolic process; cellular lipid metabolic process
Disease: Bile Acid Synthesis Defect, Congenital, 4; Alpha-methylacyl-coa Racemase Deficiency
Research Articles on aMACR
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Product Notes
The Human aMACR amacr (Catalog #AAA2000355) is an ELISA Kit and is intended for research purposes only. The product is available for immediate purchase. The AAA2000355 ELISA Kit recognizes Human aMACR. It is sometimes possible for the material contained within the vial of "Alpha-Methylacyl Coenzyme A Racemase (aMACR), ELISA Kit" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.Precautions
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