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ELOVL4 antibody (C-Term)

This Rabbit Polyclonal antibody specifically detects ELOVL4 in WB. It exhibits reactivity toward Human.
Catalog No. ABIN5536049

Quick Overview for ELOVL4 antibody (C-Term) (ABIN5536049)

Target

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

Reactivity

  • 35
  • 16
  • 11
  • 5
  • 2
  • 2
Human

Host

  • 36
Rabbit

Clonality

  • 36
Polyclonal

Conjugate

  • 18
  • 5
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ELOVL4 antibody is un-conjugated

Application

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  • 7
  • 5
  • 4
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 7
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    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 286-314, C-Term

    Purification

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

    Immunogen

    This ELOVL4 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 286-314 amino acids from the C-terminal region of human ELOVL4.

    Isotype

    Ig Fraction
  • Application Notes

    For WB starting dilution is: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5 mg/mL

    Buffer

    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

    Storage Comment

    Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • 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.

    Molecular Weight

    37 kDa

    Gene ID

    6785

    UniProt

    Q9GZR5
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