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MFN2 antibody (AA 447-476)

This anti-MFN2 antibody is a Rabbit Polyclonal antibody detecting MFN2 in WB, IHC, ELISA and FACS. Suitable for Human.
Catalog No. ABIN3031818

Quick Overview for MFN2 antibody (AA 447-476) (ABIN3031818)

Target

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

Reactivity

  • 65
  • 34
  • 31
  • 6
  • 4
  • 4
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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

Application

  • 63
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  • 17
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  • 5
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  • 1
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Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Flow Cytometry (FACS)
  • Binding Specificity

    • 18
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    AA 447-476

    Cross-Reactivity (Details)

    Expected species reactivity: Mouse, Rat

    Purification

    Antigen affinity purified

    Immunogen

    A portion of amino acids 447-476 from the human protein was used as the immunogen for this MFN2 antibody.

    Isotype

    Ig Fraction
  • Application Notes

    Titration of the MFN2 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000,IHC (Paraffin): 1:50-1:100,Flow Cytometry: 1:10-1:50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    In 1X PBS, pH 7.4, with 0.09 % sodium azide

    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

    Aliquot the MFN2 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • Target

    MFN2 (Mitofusin 2 (MFN2))

    Alternative Name

    MFN2

    Background

    MFN2 is 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.

    UniProt

    O95140

    Pathways

    Skeletal Muscle Fiber Development
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