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MIPEP antibody (AA 357-713)

The Rabbit Polyclonal anti-MIPEP antibody is suitable to detect MIPEP in samples from Human, Rat and Mouse. It has been validated for WB, ELISA, FACS and IHC (p).
Catalog No. ABIN7874283
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for MIPEP antibody (AA 357-713) (ABIN7874283)

Target

See all MIPEP Antibodies
MIPEP (Mitochondrial Intermediate Peptidase (MIPEP))

Reactivity

Human, Rat, Mouse

Host

  • 18
  • 11
Rabbit

Clonality

  • 18
  • 11
Polyclonal

Conjugate

  • 19
  • 2
  • 2
  • 2
  • 2
  • 2
This MIPEP antibody is un-conjugated

Application

  • 27
  • 17
  • 15
  • 7
  • 4
  • 3
  • 2
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Binding Specificity

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

    Purpose

    MIPEP Antibody / Mitochondrial intermediate peptidase

    Purification

    Antigen affinity chromatography

    Immunogen

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

    Isotype

    IgG
  • Application Notes

    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

    Storage

    4 °C,-20 °C

    Storage Comment

    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.
  • Target

    MIPEP (Mitochondrial Intermediate Peptidase (MIPEP))

    Alternative Name

    MIPEP

    Background

    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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