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ELOVL4 antibody (AA 1-312)

The Rabbit Polyclonal anti-ELOVL4 antibody is suitable to detect ELOVL4 in samples from Mouse and Rat. It has been validated for WB, ELISA, IF and FACS.
Catalog No. ABIN7869180
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for ELOVL4 antibody (AA 1-312) (ABIN7869180)

Target

See all ELOVL4 Antibodies
ELOVL4 (ELOVL Fatty Acid Elongase 4 (ELOVL4))

Reactivity

  • 36
  • 16
  • 11
  • 5
  • 2
  • 2
Mouse, Rat

Host

  • 37
Rabbit

Clonality

  • 37
Polyclonal

Conjugate

  • 19
  • 5
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ELOVL4 antibody is un-conjugated

Application

  • 27
  • 24
  • 7
  • 5
  • 4
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunofluorescence (IF), Flow Cytometry (FACS)
  • Binding Specificity

    • 8
    • 6
    • 5
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-312

    Purpose

    Elovl4 Antibody

    Purification

    Affinity purified

    Immunogen

    An E. coli-derived mouse protein (amino acids M1-E312) was used as the immunogen for the Elovl4 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the Elovl4 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 Elovl4 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

    ELOVL4 (ELOVL Fatty Acid Elongase 4 (ELOVL4))

    Alternative Name

    Elovl4

    Background

    Elongation of very long chain fatty acids protein 4 is a protein that in humans is encoded by the ELOVL4 gene. This gene encodes a membrane-bound protein which is a member of the ELO family, proteins which participate in the biosynthesis of fatty acids. Consistent with the expression of the encoded protein in photoreceptor cells of the retina, mutations and small deletions in this gene are associated with Stargardt-like macular dystrophy (STGD3) and autosomal dominant Stargardt-like macular dystrophy (ADMD), also referred to as autosomal dominant atrophic macular degeneration.

    UniProt

    Q9EQC4
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