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AFG3L2 antibody (N-Term)

The Rabbit Polyclonal anti-AFG3L2 antibody has been validated for WB and IHC (p). It is suitable to detect AFG3L2 in samples from Human.
Catalog No. ABIN657143

Quick Overview for AFG3L2 antibody (N-Term) (ABIN657143)

Target

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

Reactivity

  • 40
  • 7
  • 7
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 38
  • 3
Rabbit

Clonality

  • 40
  • 1
Polyclonal

Conjugate

  • 21
  • 5
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This AFG3L2 antibody is un-conjugated

Application

  • 31
  • 22
  • 21
  • 6
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

RB33011
  • Binding Specificity

    • 7
    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 52-80, N-Term

    Predicted Reactivity

    B, M

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This AFG3L2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 52-80 amino acids from the N-terminal region of human AFG3L2.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000. IHC-P: 1:10~50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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

    4 °C,-20 °C

    Expiry Date

    6 months
  • Target

    AFG3L2 (AFG3-Like Protein 2 (AFG3L2))

    Alternative Name

    AFG3L2

    Background

    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. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders.

    Molecular Weight

    88584

    NCBI Accession

    NP_006787

    UniProt

    Q9Y4W6

    Pathways

    Skeletal Muscle Fiber Development
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