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Mitofusin 2 (MFN2) Peptide

MFN2 Reactivité: Mammifères Hôte: Synthetic BP, WB, IHC
N° du produit ABIN940309

Aperçu rapide pour Mitofusin 2 (MFN2) Peptide (ABIN940309)

Antigène

MFN2 (Mitofusin 2 (MFN2))

Origine

Mammifères

Source

  • 6
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
  • Type de proteíne

    Synthetic

    Séquence

    LEQEIAAMNK KIEVLDSLQS KAKLLRNKAG WLDSELNMFT HQYLQPSR

    Attributs du produit

    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

    Purification

    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.
  • Indications d'application

    Optimal conditions should be determined by the investigator

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

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

    Buffer

    PBS

    Conseil sur la manipulation

    Avoid repeated freeze/thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20 °C long term.
  • Antigène

    MFN2 (Mitofusin 2 (MFN2))

    Sujet

    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.

    Poids moléculaire

    86 kDa
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