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Mitofusin 2 (MFN2) Peptid

MFN2 Reaktivität: Säugetier Wirt: Synthetic BP, WB, IHC
Produktnummer ABIN940309

Kurzübersicht für Mitofusin 2 (MFN2) Peptid (ABIN940309)

Target

MFN2 (Mitofusin 2 (MFN2))

Spezies

Säugetier

Quelle

  • 6
Synthetic

Applikation

Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
  • Protein-Typ

    Synthetic

    Sequenz

    LEQEIAAMNK KIEVLDSLQS KAKLLRNKAG WLDSELNMFT HQYLQPSR

    Produktmerkmale

    A synthetic peptide for use as a blocking control in assays to test for specificity of MFN2 antibody,
    Alternative Names: Mitofusin 2 control peptide, Mitofusin 2 antibody Blocking Peptide, Anti-Mitofusin 2 Blocking Peptide, CMT2A Blocking Peptide, CMT2A2 Blocking Peptide, CPRP1 Blocking Peptide, HSG Blocking Peptide, KIAA0214 Blocking Peptide, MARF Blocking Peptide, MFN2 Blocking Peptide, Mitofusin 2, Mitofusin -2, Mitofusin 2, Mitofusin -2 Blocking Peptide, Mitofusin 2 Blocking Peptide

    Aufreinigung

    The antibody is affinity purified from rabbit antiserum by affinity chromatography using epitope-specific phosphopeptide. The antibody against non-phosphopeptide is removed by chromatogramphy using non-phosphopeptide corresponding to the phosphorylation site.
  • Applikationshinweise

    Optimal conditions should be determined by the investigator

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.

    Buffer

    PBS

    Handhabung

    Avoid repeated freeze/thaw cycles.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store at -20 °C long term.
  • Target

    MFN2 (Mitofusin 2 (MFN2))

    Hintergrund

    MFN2 is a mitochondrial membrane protein that participates in mitochondrial fusion and contributes to the maintenance and operation of the mitochondrial network. It is involved in the regulation of vascular smooth muscle cell proliferation, and it may play a role in the pathophysiology of obesity. Mutations in this gene cause Charcot-Marie-Tooth disease type 2A2, and hereditary motor and sensory neuropathy VI, which are both disorders of the peripheral nervous system. Defects in this gene have also been associated with early-onset stroke.

    Molekulargewicht

    86 kDa
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