Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

NPHP3 anticorps (AA 1092-1142)

L’anticorps anti-NPHP3 Polyclonal Lapin est utilisé pour la détection de NPHP3 dans des échantillons de Humain et Souris. Il a été validé pour WB.
N° du produit ABIN8123265
450,00 €
Plus frais de livraison 40,00 € et TVA
50 μL
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour NPHP3 anticorps (AA 1092-1142) (ABIN8123265)

Antigène

Voir toutes NPHP3 Anticorps
NPHP3 (Nephronophthisis 3 (Adolescent) (NPHP3))

Reactivité

Humain, Souris

Hôte

  • 16
  • 1
Lapin

Clonalité

  • 16
  • 1
Polyclonal

Conjugué

  • 12
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp NPHP3 est non-conjugé

Application

  • 16
  • 12
  • 10
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 8
    • 3
    • 3
    • 2
    • 1
    • 1
    AA 1092-1142

    Fonction

    NPHP3 Antibody

    Specificité

    This antibody detects endogenous levels of NPHP3 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 NPHP3 AA range: 1092-1142

    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

    NPHP3 (Nephronophthisis 3 (Adolescent) (NPHP3))

    Autre désignation

    NPHP3

    Sujet

    Background: This gene encodes a protein containing a coiled-coil (CC) domain, a tubulin-tyrosine ligase (TTL) domain, and a tetratrico peptide repeat (TPR) domain. The encoded protein interacts with nephrocystin, it is required for normal ciliary development, and it functions in renal tubular development. Mutations in this gene are associated with nephronophthisis type 3, and also with renal-hepatic-pancreatic dysplasia, and Meckel syndrome type 7. Naturally occurring read-through transcripts exist between this gene and the downstream ACAD11 (acyl-CoA dehydrogenase family, member 11) gene. [provided by RefSeq, Feb 2011],

    Gene Name: NPHP3 KIAA2000

    Protein Name: NPHP3

    ID gène

    27031

    UniProt

    Q7Z494

    Pathways

    cAMP Metabolic Process
Vous êtes ici:
Chat with us!