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ELOVL4 Antikörper (C-Term)

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch ELOVL4 in WB. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN5536049

Kurzübersicht für ELOVL4 Antikörper (C-Term) (ABIN5536049)

Target

Alle ELOVL4 Antikörper anzeigen
ELOVL4 (ELOVL Fatty Acid Elongase 4 (ELOVL4))

Reaktivität

  • 36
  • 16
  • 11
  • 5
  • 2
  • 2
Human

Wirt

  • 37
Kaninchen

Klonalität

  • 37
Polyklonal

Konjugat

  • 19
  • 5
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser ELOVL4 Antikörper ist unkonjugiert

Applikation

  • 27
  • 25
  • 8
  • 6
  • 4
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Bindungsspezifität

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

    Aufreinigung

    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.

    Isotyp

    Ig Fraction
  • Applikationshinweise

    For WB starting dilution is: 1:1000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    0.5 mg/mL

    Buffer

    Supplied in PBS with 0.09 % (W/V) sodium azide.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

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

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    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))

    Andere Bezeichnung

    ELOVL4

    Hintergrund

    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.

    Molekulargewicht

    37 kDa

    Gen-ID

    6785

    UniProt

    Q9GZR5
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