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ELOVL4 anticorps (AA 1-312)

L’anticorps anti-ELOVL4 Polyclonal Lapin est utilisé pour la détection de ELOVL4 dans des échantillons de Souris et Rat. Il a été validé pour WB, ELISA, IF et FACS.
N° du produit ABIN7869180
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour ELOVL4 anticorps (AA 1-312) (ABIN7869180)

Antigène

Voir toutes ELOVL4 Anticorps
ELOVL4 (ELOVL Fatty Acid Elongase 4 (ELOVL4))

Reactivité

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

Hôte

  • 37
Lapin

Clonalité

  • 37
Polyclonal

Conjugué

  • 19
  • 5
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp ELOVL4 est non-conjugé

Application

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

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

    Fonction

    Elovl4 Antibody

    Purification

    Affinity purified

    Immunogène

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

    Isotype

    IgG
  • Indications d'application

    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

    Stock

    4 °C,-20 °C

    Stockage commentaire

    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.
  • Antigène

    ELOVL4 (ELOVL Fatty Acid Elongase 4 (ELOVL4))

    Autre désignation

    Elovl4

    Sujet

    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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