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Rabbit anti-Human MCEE Polyclonal Antibody

The antibody against MCEE was raised in rabbit using the Human MCEE as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB.

ADC-52783A

The antibody against MCEE was raised in rabbit using the Human MCEE as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB.

$600.00

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Specifications


Cat.No ADC-52783A ClonalityPolyclonal
Host SpeciesRabbitTarget NameMCEE
FormLiquidSpecies ReactivityHuman, Mouse, Rat
IsotypeIgGStorage Buffer50% Glycerol, Avoid freeze / thaw cycles., PBS with 0.1% Sodium Azide
Purification MethodAntigen affinity purifiedConjugateNon-conjugated
ApplicationELISA, WBStorageUpon receipt

Immunogen Information


Immunogen DescriptionHuman MCEETarget SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDQ96PE7
Background Information
  • Uniprot Id

    Q96PE7

  • Target Species

    Human

  • Target Name

    MCEE

  • Target Full Name

    Methylmalonyl-CoA epimerase, mitochondrial

  • Target Function

    Methylmalonyl-CoA epimerase involved in propionyl-CoA metabolism.

  • Target Involvement

    Methylmalonyl-CoA epimerase deficiency (MCEED)

  • Target Subcellular Location

    Mitochondrion.

  • Target Protein Families

    Glyoxalase I family

  • Target Synonyms

    DL methylmalonyl CoA racemase; DL-methylmalonyl-CoA racemase; EC 5.1.99.1; GLOD2 ; Glyoxalase domain containing 2 ; MCEE; MCEE_HUMAN; Methylmalonyl CoA epimerase; Methylmalonyl-CoA epimerase; methylmalonyl-CoA epimerase; mitochondrial; mitochondrial; OTTHUMP00000160122

  • Target Background

    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.

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