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Rabbit polyclonal to MCEE
Synthetic peptide conjugated to KLH, between amino acids 135-164 from the C-terminal region of Human MCEE (NP_115990.3).
Mouse liver tissue lysate
Shipped at 4°C. Store at 4°C (up to 6 months). Store at -20°C long term.
Preservative: 0.09% Sodium Azide
Concentration information loading...
Immunogen affinity purified
ab107537 is purified through a protein A column, followed by peptide affinity purification.
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in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
1/100 - 1/500. Predicted molecular weight: 19 kDa.
Involvement in disease
Defects in MCEE are a cause of methylmalonyl-CoA epimerase deficiency (MCEE deficiency) [MIM:251120]; also known as methylmalonyl-CoA racemase deficiency or methylmalonic aciduria type 3. MCEE deficiency is an autosomal recessive inborn error of amino acid metabolism, involving valine, threonine, isoleucine and methionine. This organic aciduria may present in the neonatal period with life-threatening metabolic acidosis, hyperammonemia, feeding difficulties, pancytopenia and coma.
Belongs to the glyoxalase I family.
Information by UniProt
DL methylmalonyl CoA racemase antibody
DL-methylmalonyl-CoA racemase antibody
EC 18.104.22.168 antibody
has not yet been referenced specifically in any publications.
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