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NIPBL anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement NIPBL dans ELISA et IHC. Il présente une réactivité envers Humain et Souris.
N° du produit ABIN7246814

Aperçu rapide pour NIPBL anticorps (ABIN7246814)

Antigène

Voir toutes NIPBL Anticorps
NIPBL (Nipped-B like Protein (NIPBL))

Reactivité

  • 16
  • 15
  • 5
Humain, Souris

Hôte

  • 24
  • 3
  • 3
  • 1
Lapin

Clonalité

  • 27
  • 4
Polyclonal

Conjugué

  • 13
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp NIPBL est non-conjugé

Application

  • 13
  • 13
  • 9
  • 9
  • 5
  • 5
  • 4
  • 3
  • 3
  • 2
ELISA, Immunohistochemistry (IHC)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogène

    Fusion protein of human NIPBL

    Isotype

    IgG
  • Indications d'application

    IHC 1:50-1:200, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.9 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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. Avoid freeze / thaw cycles.
  • Antigène

    NIPBL (Nipped-B like Protein (NIPBL))

    Autre désignation

    NIPBL

    Sujet

    This gene encodes the homolog of the Drosophila melanogaster Nipped-B gene product and fungal Scc2-type sister chromatid cohesion proteins. The Drosophila protein facilitates enhancer-promoter communication of remote enhancers and plays a role in developmental regulation. It is also homologous to a family of chromosomal adherins with broad roles in sister chromatid cohesion, chromosome condensation, and DNA repair. The human protein has a bipartite nuclear targeting sequence and a putative HEAT repeat. Condensins, cohesins and other complexes with chromosome-related functions also contain HEAT repeats. Mutations in this gene result in Cornelia de Lange syndrome, a disorder characterized by dysmorphic facial features, growth delay, limb reduction defects, and cognitive disability. Two transcript variants encoding different isoforms have been found for this gene.

    UniProt

    Q6KC79

    Pathways

    Sensory Perception of Sound, Stem Cell Maintenance
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