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MIPEP anticorps (AA 357-713)

L’anticorps anti-MIPEP Polyclonal Lapin est utilisé pour la détection de MIPEP dans des échantillons de Humain, Rat et Souris. Il a été validé pour WB, ELISA, FACS et IHC (p).
N° du produit ABIN7874283
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour MIPEP anticorps (AA 357-713) (ABIN7874283)

Antigène

Voir toutes MIPEP Anticorps
MIPEP (Mitochondrial Intermediate Peptidase (MIPEP))

Reactivité

Humain, Rat, Souris

Hôte

  • 18
  • 10
Lapin

Clonalité

  • 18
  • 10
Polyclonal

Conjugué

  • 18
  • 2
  • 2
  • 2
  • 2
  • 2
Cet anticorp MIPEP est non-conjugé

Application

  • 26
  • 16
  • 15
  • 7
  • 4
  • 3
  • 2
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Épitope

    • 7
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 357-713

    Fonction

    MIPEP Antibody / Mitochondrial intermediate peptidase

    Purification

    Antigen affinity chromatography

    Immunogène

    An E.coli-derived human recombinant protein (amino acids D357-E713) was used as the immunogen for the MIPEP antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the MIPEP antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Stock

    4 °C,-20 °C

    Stockage commentaire

    After reconstitution, the MIPEP Antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Antigène

    MIPEP (Mitochondrial Intermediate Peptidase (MIPEP))

    Autre désignation

    MIPEP

    Sujet

    Mitochondrial intermediate peptidase is an enzyme that in humans is encoded by the MIPEP gene. 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.

    UniProt

    Q99797
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