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Nyctalopin anticorps (AA 139-189)

Cet anticorps Lapin Polyclonal détecte spécifiquement Nyctalopin dans WB. Il présente une réactivité avec des échantillons de Humain et Souris.
N° du produit ABIN8123495
450,00 €
Plus frais de livraison 40,00 € et TVA
50 μL
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour Nyctalopin anticorps (AA 139-189) (ABIN8123495)

Antigène

Voir toutes Nyctalopin (NYX) Anticorps
Nyctalopin (NYX)

Reactivité

Humain, Souris

Hôte

  • 12
Lapin

Clonalité

  • 12
Polyclonal

Conjugué

  • 7
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Nyctalopin est non-conjugé

Application

  • 12
  • 9
  • 2
  • 1
Western Blotting (WB)
  • Épitope

    • 8
    • 3
    • 2
    • 2
    AA 139-189

    Fonction

    NYX Antibody

    Specificité

    This antibody detects endogenous levels of NYX at Human/Mouse

    Purification

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

    Immunogène

    Synthesized peptide derived from human NYX AA range: 139-189

    Isotype

    IgG
  • Indications d'application

    WB 1:500-2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C/1 year

    Date de péremption

    12 months
  • Antigène

    Nyctalopin (NYX)

    Autre désignation

    NYX

    Sujet

    Background: The product of this gene belongs to the small leucine-rich proteoglycan (SLRP) family of proteins. Defects in this gene are the cause of congenital stationary night blindness type 1 (CSNB1), also called X-linked congenital stationary night blindness (XLCSNB). CSNB1 is a rare inherited retinal disorder characterized by impaired scotopic vision, myopia, hyperopia, nystagmus and reduced visual acuity. The role of other SLRP proteins suggests that mutations in this gene disrupt developing retinal interconnections involving the ON-bipolar cells, leading to the visual losses seen in patients with complete CSNB. [provided by RefSeq, Oct 2008],

    Gene Name: NYX CLRP

    Protein Name: NYX

    ID gène

    60506

    UniProt

    Q9GZU5
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