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ELOVL4 antibody (C-Term)

This Rabbit Polyclonal antibody specifically detects ELOVL4 in WB and EIA. It exhibits reactivity toward Human.
Catalog No. ABIN952069

Quick Overview for ELOVL4 antibody (C-Term) (ABIN952069)

Target

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

Reactivity

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  • 16
  • 11
  • 5
  • 2
  • 2
Human

Host

  • 37
Rabbit

Clonality

  • 37
Polyclonal

Conjugate

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

Application

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  • 1
  • 1
Western Blotting (WB), Enzyme Immunoassay (EIA)
  • Binding Specificity

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    • 1
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    • 1
    AA 285-314, C-Term

    Specificity

    This antibody recognizes Human ELOVL4 (C-term).

    Purification

    Affinity Chromatography on Protein A

    Immunogen

    KLH conjugated synthetic peptide between 285-314 amino acids from the C-terminal region of Human ELOVL4.

    Isotype

    Ig Fraction
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.25 mg/mL

    Buffer

    PBS containing 0.09 % (W/V) sodium azide as preservative

    Preservative

    Sodium azide

    Precaution of Use

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target

    ELOVL4 (ELOVL Fatty Acid Elongase 4 (ELOVL4))

    Alternative Name

    ELOVL4

    Background

    ELOVL4 is 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.Synonyms: 3-keto acyl-CoA synthase ELOVL4, Elongation of very long chain fatty acids protein 4

    Molecular Weight

    36829 Da

    Gene ID

    6785

    NCBI Accession

    NP_073563
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