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MFN2 Antikörper

Der Kaninchen Monoklonal Anti-MFN2 Antikörper wurde für WB validiert. Er ist geeignet, MFN2 in Proben von Human zu detektieren.
Produktnummer ABIN7268606

Kurzübersicht für MFN2 Antikörper (ABIN7268606)

Target

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

Reaktivität

  • 76
  • 42
  • 39
  • 6
  • 4
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Wirt

  • 64
  • 26
  • 2
Kaninchen

Klonalität

  • 54
  • 38
Monoklonal

Konjugat

  • 45
  • 7
  • 6
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser MFN2 Antikörper ist unkonjugiert

Applikation

  • 74
  • 54
  • 33
  • 27
  • 26
  • 13
  • 7
  • 6
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Verwendungszweck

    Mitofusin 2 Rabbit mAb

    Kreuzreaktivität

    Human, Maus, Ratte

    Produktmerkmale

    Monoclonal Antibodies

    Aufreinigung

    Affinity purification

    Immunogen

    A synthesized peptide derived from human Mitofusin 2.

    Isotyp

    IgG
  • Applikationshinweise

    WB,1:500 - 1:2000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    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

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    MFN2 (Mitofusin 2 (MFN2))

    Andere Bezeichnung

    MFN2

    Hintergrund

    This gene encodes 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, which are both 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. [provided by RefSeq, Jul 2008],CMT2A,CMT2A2,CMT2A2A,CMT2A2B,CPRP1,HMSN6A,HSG,MARF,MFN2,Mitofusin 2,Apoptosis,Autophagy,Autophagy_Mitochondrial Control of Autophagy,Cancer,Cell Biology & Developmental Biology,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial metabolism_Mitochondrial markers,Mitochondrial metabolism_Mitophagy fission and fusion,Neurodegenerative Diseases,Neuroscience,Signal Transduction,MFN2

    Molekulargewicht

    80kDa

    Gen-ID

    9927

    UniProt

    O95140

    Pathways

    Skeletal Muscle Fiber Development
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