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MFN2 antibody (C-Term)

This anti-MFN2 antibody is a Rabbit Polyclonal antibody detecting MFN2 in WB. Suitable for Human and Rat.
Catalog No. ABIN635034

Quick Overview for MFN2 antibody (C-Term) (ABIN635034)

Target

See all MFN2 Antibodies
MFN2 (Mitofusin 2 (MFN2))

Reactivity

  • 68
  • 33
  • 31
  • 6
  • 4
  • 4
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
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Human, Rat

Host

  • 58
  • 26
  • 2
Rabbit

Clonality

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  • 30
Polyclonal

Conjugate

  • 48
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  • 4
  • 4
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  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This MFN2 antibody is un-conjugated

Application

  • 66
  • 48
  • 34
  • 18
  • 17
  • 13
  • 6
  • 5
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 18
    • 7
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    • 5
    • 5
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    • 2
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    • 2
    • 1
    • 1
    • 1
    • 1
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    • 1
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    • 1
    C-Term

    Specificity

    Mitofusin 2 antibody was raised against the C terminal of MFN2

    Purification

    Affinity purified

    Immunogen

    Mitofusin 2 antibody was raised using the C terminal of MFN2 corresponding to a region with amino acids LEQEIAAMNKKIEVLDSLQSKAKLLRNKAGWLDSELNMFTHQYLQPSR
  • Application Notes

    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.

    Comment

    Mitofusin 2 Blocking Peptide, (ABIN940309), is also available for use as a blocking control in assays to test for specificity of this Mitofusin 2 antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of MFN2 antibody in PBS

    Concentration

    Lot specific

    Buffer

    PBS

    Handling Advice

    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • Target

    MFN2 (Mitofusin 2 (MFN2))

    Alternative Name

    Mitofusin 2

    Background

    MFN2 is a mitochondrial membrane protein that participates in mitochondrial fusion and contributes to the maintenance and operation of the mitochondrial network. It 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.

    Molecular Weight

    86 kDa (MW of target protein)

    Pathways

    Skeletal Muscle Fiber Development
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