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Rabbit anti-Human MIPEP Polyclonal Antibody

The antibody against MIPEP was raised in rabbit using the Recombinant Human Mitochondrial intermediate peptidase protein (504-713AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IHC.

ADC-16650A

The antibody against MIPEP was raised in rabbit using the Recombinant Human Mitochondrial intermediate peptidase protein (504-713AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IHC.

$299.00

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Specifications


Cat.No ADC-16650A ClonalityPolyclonal
Host SpeciesRabbitTarget NameMIPEP
FormLiquidSpecies ReactivityHuman
IsotypeIgGStorage Buffer50% Glycerol, PBS with 0.02% sodium azide, pH7.3.
Purification MethodAntigen affinity purifiedConjugateNon-conjugated
ApplicationELISA, IHCStorageUpon receipt

Immunogen Information


Immunogen DescriptionRecombinant Human Mitochondrial intermediate peptidase protein (504-713AA)Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDQ99797
Background Information
  • Uniprot Id

    Q99797

  • Target Species

    Human

  • Target Name

    MIPEP

  • Target Full Name

    Mitochondrial intermediate peptidase

  • Target Function

    Cleaves proteins, imported into the mitochondrion, to their mature size.

  • Target Involvement

    Combined oxidative phosphorylation deficiency 31 (COXPD31)

  • Target Subcellular Location

    Mitochondrion matrix.

  • Target Protein Families

    Peptidase M3 family

  • Target Synonyms

    EC 3.4.24.59 ; HMIP; MIP; Mipep; MIPEP_HUMAN; Mitochondrial intermediate peptidase; Mitochondrial intermedieate peptide; OTTHUMP00000018121; OTTHUMP00000042292

  • Target Background

    The product of this gene performs the final step in processing a specific class of nuclear-encoded proteins targeted to the mitochondrial matrix or inner membrane. This protein is primarily involved in the maturation of oxidative phosphorylation (OXPHOS)-related proteins. This gene may contribute to the functional effects of frataxin deficiency and the clinical manifestations of Friedreich ataxia.

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