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OPA1 antibody

OPA1 Reactivity: Human, Mouse, Rat WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN6572036
  • Target See all OPA1 Antibodies
    OPA1 (Optic Atrophy 1 (Autosomal Dominant) (OPA1))
    Reactivity
    • 45
    • 28
    • 28
    • 17
    • 17
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 41
    • 4
    Rabbit
    Clonality
    • 36
    • 9
    Polyclonal
    Conjugate
    • 18
    • 4
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This OPA1 antibody is un-conjugated
    Application
    • 29
    • 13
    • 13
    • 13
    • 4
    • 4
    • 3
    • 1
    Western Blotting (WB)
    Purification
    Affinity purification
    Immunogen
    Recombinant protein of human OPA1
    Isotype
    IgG
    Top Product
    Discover our top product OPA1 Primary Antibody
  • Application Notes
    WB 1:500 - 1:2000
    Restrictions
    For Research Use only
  • Concentration
    1 mg/mL
    Buffer
    Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    OPA1 (Optic Atrophy 1 (Autosomal Dominant) (OPA1))
    Alternative Name
    OPA1 (OPA1 Products)
    Background

    Synonyms: Dynamin like 120 kDa protein,Dynamin like 120 kDa protein, mitochondrial,Dynamin-like 120 kDa protein, form S1,FLJ12460,Juvenile kjer type optic atrophy,KIAA0567,KJER type,Large GTP binding protein,largeG,MGM1,Mitochondrial dynamin like 120 kDa protein,Mitochondrial dynamin like GTPase,NPG,NTG,OAK,OPA 1,opa1,OPA1 gene,OPA1,Optic atrophy 1 (autosomal dominant),OPTIC ATROPHY 1,Optic atrophy 1 gene protein,Optic atrophy 1 homolog (human),Optic atrophy protein 1,Optic atrophy protein 1 homolog

    Background: This gene product is a nuclear-encoded mitochondrial protein with similarity to dynamin-related GTPases. It is a component of the mitochondrial network. Mutations in this gene have been associated with optic atrophy type 1, which is a dominantly inherited optic neuropathy resulting in progressive loss of visual acuity, leading in many cases to legal blindness. Multiple transcript variants encoding different isoforms have been found for this gene.

    Molecular Weight

    Observed_MW: 112kDa

    Calculated_MW: 111kDa/115kDa

    Gene ID
    4976
    UniProt
    O60313
    Pathways
    Tube Formation
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