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OCRL anticorps (AA 1-901)

L’anticorps anti-OCRL Polyclonal Lapin est utilisé pour la détection de OCRL dans des échantillons de Humain. Il a été validé pour WB, ELISA, IHC (p) et IF.
N° du produit ABIN7869609
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour OCRL anticorps (AA 1-901) (ABIN7869609)

Antigène

Voir toutes OCRL Anticorps
OCRL (Oculocerebrorenal Syndrome of Lowe (OCRL))

Reactivité

  • 22
  • 5
  • 1
  • 1
Humain

Hôte

  • 16
  • 7
Lapin

Clonalité

  • 19
  • 4
Polyclonal

Conjugué

  • 19
  • 2
  • 1
  • 1
Cet anticorp OCRL est non-conjugé

Application

  • 18
  • 13
  • 7
  • 4
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (IF)
  • Épitope

    • 5
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-901

    Fonction

    OCRL-1 Antibody

    Purification

    Antigen affinity purified

    Immunogène

    E. coli-derived recombinant human protein (amino acids M1-D901) was used as the immunogen for the OCRL-1 antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the OCRL-1 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 OCRL-1 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

    OCRL (Oculocerebrorenal Syndrome of Lowe (OCRL))

    Autre désignation

    OCRL-1

    Sujet

    Inositol polyphosphate 5-phosphatase OCRL-1, also known as Lowe oculocerebrorenal syndrome protein, is an enzyme encoded by the OCRL gene located on the X chromosome in humans. This gene encodes an inositol polyphosphate 5-phosphatase. This protein is involved in regulating membrane trafficking and is located in numerous subcellular locations including the trans-Golgi network, clathrin-coated vesicles and endosomes and the plasma membrane. This protein may also play a role in primary cilium formation. Mutations in this gene cause oculocerebrorenal syndrome of Lowe and also Dent disease. Alternate splicing results in multiple transcript variants.

    UniProt

    Q01968

    Pathways

    Inositol Metabolic Process
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