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Rabbit anti-Human MTIF3 Polyclonal Antibody

The antibody against MTIF3 was raised in rabbit using the Human MTIF3 as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB.

ADC-52671A

The antibody against MTIF3 was raised in rabbit using the Human MTIF3 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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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ADC-52671A ClonalityPolyclonal
Host SpeciesRabbitTarget NameMTIF3
FormLiquidSpecies ReactivityHuman
IsotypeIgGStorage Buffer50% Glycerol, Avoid freeze / thaw cycles., PBS with 0.02% sodium azide
Purification MethodAntigen affinity purifiedConjugateNon-conjugated
ApplicationELISA, WBStorageUpon receipt

Immunogen Information


Immunogen DescriptionHuman MTIF3Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDQ9H2K0
Background Information
  • Uniprot Id

    Q9H2K0

  • Target Species

    Human

  • Target Name

    MTIF3

  • Target Full Name

    Translation initiation factor IF-3, mitochondrial

  • Target Function

    IF-3 binds to the 28S ribosomal subunit and shifts the equilibrum between 55S ribosomes and their 39S and 28S subunits in favor of the free subunits, thus enhancing the availability of 28S subunits on which protein synthesis initiation begins.

  • Target Subcellular Location

    Mitochondrion.

  • Target Protein Families

    IF-3 family

  • Target Research Area

    Neuroscience

  • Target Synonyms

    DC38; IF 3 ; IF 3Mt; IF-3(Mt); IF-3Mt; IF3 ; IF3(mt); IF3M_HUMAN; IF3mt; mitochondrial; Mt; MTIF3; Translation initiation factor IF 3; mitochondrial precursor; Translation initiation factor IF-3

  • Target Background

    This gene encodes a translation initiation factor that is involved in mitochondrial protein synthesis. Polymorphism in this gene is associated with the onset of Parkinson's disease. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 5.

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