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OPA1 antibody

This anti-OPA1 antibody is a Rabbit Polyclonal antibody detecting OPA1 in WB. Suitable for Human, Rat and Mouse.
Catalog No. ABIN6572036

Quick Overview for OPA1 antibody (ABIN6572036)

Target

See all OPA1 Antibodies
OPA1 (Optic Atrophy 1 (Autosomal Dominant) (OPA1))

Reactivity

  • 50
  • 33
  • 31
  • 17
  • 17
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human, Rat, Mouse

Host

  • 49
  • 4
Rabbit

Clonality

  • 43
  • 10
Polyclonal

Conjugate

  • 26
  • 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

  • 36
  • 14
  • 13
  • 13
  • 10
  • 8
  • 4
  • 4
  • 3
  • 3
  • 3
Western Blotting (WB)
  • Purification

    Affinity purification

    Immunogen

    Recombinant protein of human OPA1

    Isotype

    IgG
  • 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

    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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