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FANCD2 anticorps

Cet anticorps Lapin Monoclonal détecte spécifiquement FANCD2 dans WB. Il présente une réactivité envers Humain.
N° du produit ABIN7267126

Aperçu rapide pour FANCD2 anticorps (ABIN7267126)

Antigène

Voir toutes FANCD2 Anticorps
FANCD2 (Fanconi Anemia, Complementation Group D2 (FANCD2))

Reactivité

  • 68
  • 25
  • 22
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 68
  • 1
Lapin

Clonalité

  • 59
  • 10
Monoclonal

Conjugué

  • 29
  • 5
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp FANCD2 est non-conjugé

Application

  • 25
  • 21
  • 19
  • 14
  • 14
  • 14
  • 7
  • 7
  • 7
  • 6
  • 4
  • 1
  • 1
Western Blotting (WB)
  • Fonction

    FANCD2 Rabbit mAb

     Réactivité croisée

    Humain, Souris, Rat

    Attributs du produit

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogène

    A synthesized peptide derived from human FANCD2.

    Isotype

    IgG
  • Indications d'application

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    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

    FANCD2 (Fanconi Anemia, Complementation Group D2 (FANCD2))

    Autre désignation

    FANCD2

    Sujet

    The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity, they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group D2. This protein is monoubiquinated in response to DNA damage, resulting in its localization to nuclear foci with other proteins (BRCA1 AND BRCA2) involved in homology-directed DNA repair. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016],FA4,FAD,FACD,FAD2,FA-D2,FANCD,FANCD2,Cell Biology & Developmental Biology,Cell Cycle,DNA Damage & Repair,Epigenetics & Nuclear Signaling,G2/M DNA Damage Checkpoint,FANCD2

    Poids moléculaire

    166kDa

    ID gène

    2177

    UniProt

    Q9BXW9

    Pathways

    Réparation de l'ADN
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