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MFN2 Antikörper (AA 370-600)

Der Maus Monoklonal Anti-MFN2-Antikörper wurde für WB, IHC und IF/ICC validiert. Er ist geeignet, MFN2 in Proben von Maus zu detektieren.
Produktnummer ABIN7233053

Kurzübersicht für MFN2 Antikörper (AA 370-600) (ABIN7233053)

Target

Alle MFN2 Antikörper anzeigen
MFN2 (Mitofusin 2 (MFN2))

Reaktivität

  • 66
  • 34
  • 30
  • 6
  • 4
  • 4
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Maus

Wirt

  • 59
  • 22
  • 2
Maus

Klonalität

  • 57
  • 26
Monoklonal

Konjugat

  • 48
  • 6
  • 5
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser MFN2 Antikörper ist unkonjugiert

Applikation

  • 63
  • 47
  • 34
  • 17
  • 15
  • 13
  • 5
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (fixed cells) (IF/ICC)

Klon

S153-5
  • Bindungsspezifität

    • 17
    • 7
    • 7
    • 5
    • 4
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 370-600

    Verwendungszweck

    Anti-Mitofusin-2 Mouse Monoclonal Antibody

    Spezifität

    This antibody recognizes human, mouse, and rat Mitofusin-2. It does not cross- react with Mitofusin-1.

    Kreuzreaktivität

    Human, Maus, Ratte

    Immunogen

    Fusion protein corresponding to aa 370-600 (cytoplasmic N-terminus) of mouse Mitofusin-2. This sequence is 97

    Isotyp

    IgG2a
  • Applikationshinweise

    Immunoblotting: use at 1-5 μg/mL. A band of ~90 kDa is detected.
    Immunofluorescence: use at 10 μg/mL.
    These are recommended concentrations.
    Enduser should determine optimal concentrations for their application.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Rekonstitution

    Dilute in PBS or medium that is identical to that used in the assay system.

    Konzentration

    1.0 mg/mL

    Buffer

    PBS, pH 7.4, 0.1 % sodium azide, 50 % glycerol.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    This product is stable for at least one (1) year at -20°C.
  • Target

    MFN2 (Mitofusin 2 (MFN2))

    Andere Bezeichnung

    Mfn2

    Hintergrund

    Mitofusin-2,Mitochondrial outer membrane GTPase that mediates mitochondrial clustering and fusion (PubMed:12527753, PubMed:23921378, PubMed:23620051). Mitochondria are highly dynamic organelles, and their morphology is determined by the equilibrium between mitochondrial fusion and fission events. Overexpression induces the formation of mitochondrial networks. Membrane clustering requires GTPase activity and may involve a major rearrangement of the coiled coil domains (By similarity). Plays a central role in mitochondrial metabolism and may be associated with obesity and/or apoptosis processes. Plays an important role in the regulation of vascular smooth muscle cell proliferation (By similarity). Involved in the clearance of damaged mitochondria via selective autophagy (mitophagy). Is required for PRKN recruitment to dysfunctional mitochondria (PubMed:23620051). Involved in the control of unfolded protein response (UPR) upon ER stress including activation of apoptosis and autophagy during ER stress (PubMed:23921556). Acts as an upstream regulator of EIF2AK3 and suppresses EIF2AK3 activation under basal conditions (PubMed:23921556). {UniProtKB:O95140, UniProtKB:Q8R500, PubMed:12527753, PubMed:23620051, PubMed:23921378, PubMed:23921556}.,Mitofusin-2 (Mfn2) is a mitochondrial membrane protein that participates in mitochondrial fusion and contributes to the maintenance and operation of the mitochondrial network. This protein 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, both of which are disorders of the peripheral nervous system. Defects in this gene have also been associated with early-onset stroke. Two transcript variants encoding the same protein have been identified.,Mitochondrion outer membrane,EC 3.6.5.-, Hypertension-related protein 1, Mitochondrial assembly regulatory factor, HSG protein, Transmembrane GTPase MFN2

    UniProt

    Q80U63

    Pathways

    Skeletal Muscle Fiber Development
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