MOCE Mouse Monoclonal Antibody [Kloon ID: LBI11G7]

The product of this gene catalyzes the interconversion of D- and L-methylmalonyl-CoA during the degradation of branched chain amino acids. odd chain-length fatty acids, and other metabolites. Mutations in this gene result in methylmalonyl-CoA epimerase deficiency, which is presented as mild to moderate methylmalonic aciduria. [provided by RefSeq, Jul 2008]

Carrier-free (BSA/glycerol-free) MCEE mouse monoclonal antibody, clone LBI11G7

GLOD2

Homo sapiens methylmalonyl-CoA epimerase (MCEE), mRNA; nuclear gene for mitochondrial product.

84693

Q96PE7

Unconjugated

Metabolic pathways, Propanoate metabolism, Valine, leucine and isoleucine degradation

Metabolic pathways, Propanoate metabolism, Valine, leucine and isoleucine degradation

WB 1:2000, IHC 1:150

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

MCEE

https://www.ncbi.nlm.nih.gov/gene/?term=84693

https://www.uniprot.org/uniprot/Q96PE7