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AFG3L2 antibody (AA 161-245)

This Rabbit Polyclonal antibody specifically detects AFG3L2 in WB. It exhibits reactivity toward Zebrafish (Danio rerio).
Catalog No. ABIN7871108
$743.31
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for AFG3L2 antibody (AA 161-245) (ABIN7871108)

Target

See all AFG3L2 Antibodies
AFG3L2 (AFG3-Like Protein 2 (AFG3L2))

Reactivity

  • 43
  • 9
  • 8
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Zebrafish (Danio rerio)

Host

  • 42
  • 3
Rabbit

Clonality

  • 44
  • 1
Polyclonal

Conjugate

  • 25
  • 5
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This AFG3L2 antibody is un-conjugated

Application

  • 34
  • 22
  • 21
  • 7
  • 5
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 8
    • 5
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 161-245

    Purpose

    Zebrafish Afg3l2 Antibody / AFG3 like protein 2

    Purification

    Antigen affinity chromatography

    Immunogen

    An E.coli-derived zebrafish Afg3l2 recombinant protein (amino acids G161-D245) was used as the immunogen for the Zebrafish Afg3l2 antibody.

    Isotype

    Ig Fraction
  • Application Notes

    Optimal dilution of the Zebrafish Afg3l2 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the Zebrafish Afg3l2 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    AFG3L2 (AFG3-Like Protein 2 (AFG3L2))

    Alternative Name

    Afg3l2

    Background

    AFG3L2 is the catalytic subunit of the m-AAA protease, an ATP-dependent proteolytic complex of the mitochondrial inner membrane that degrades misfolded proteins and regulates ribosome assembly. In humans, it is encoded by the AFG3L2 gene. This gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. And this gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders as well as spastic ataxia-neuropathy syndrome.

    UniProt

    A9JRG9

    Pathways

    Skeletal Muscle Fiber Development
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