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MFN2 anticorps

L’anticorps Lapin Monoclonal anti-MFN2 a été validé pour WB. Il convient pour détecter MFN2 dans des échantillons de Humain.
N° du produit ABIN7268606

Aperçu rapide pour MFN2 anticorps (ABIN7268606)

Antigène

Voir toutes MFN2 Anticorps
MFN2 (Mitofusin 2 (MFN2))

Reactivité

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

Hôte

  • 64
  • 26
  • 2
Lapin

Clonalité

  • 54
  • 38
Monoclonal

Conjugué

  • 45
  • 7
  • 6
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp MFN2 est non-conjugé

Application

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

    Mitofusin 2 Rabbit mAb

     Réactivité croisée

    Humain, Souris, Rat

    Attributs du produit

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogène

    A synthesized peptide derived from human Mitofusin 2.

    Isotype

    IgG
  • Indications d'application

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

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

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Stock

    -20 °C

    Stockage commentaire

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

    MFN2 (Mitofusin 2 (MFN2))

    Autre désignation

    MFN2

    Sujet

    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

    Poids moléculaire

    80kDa

    ID gène

    9927

    UniProt

    O95140

    Pathways

    Skeletal Muscle Fiber Development
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