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UFD1L anticorps (AA 208-307)

L’anticorps Souris Monoclonal anti-UFD1L a été validé pour WB, IHC, ELISA, ICC et FACS. Il convient pour détecter UFD1L dans des échantillons de Humain.
N° du produit ABIN5542401

Aperçu rapide pour UFD1L anticorps (AA 208-307) (ABIN5542401)

Antigène

Voir toutes UFD1L Anticorps
UFD1L (Ubiquitin Fusion Degradation Protein 1 Homolog (UFD1L))

Reactivité

  • 41
  • 27
  • 26
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 36
  • 4
Souris

Clonalité

  • 35
  • 6
Monoclonal

Conjugué

  • 26
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp UFD1L est non-conjugé

Application

  • 38
  • 13
  • 10
  • 9
  • 8
  • 6
  • 5
  • 5
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunocytochemistry (ICC), Flow Cytometry (FACS)

Clone

2A6F3
  • Épitope

    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 208-307

    Fonction

    UFD1L Antibody

    Purification

    Purified antibody

    Immunogène

    Purified recombinant fragment of human UFD1L (AA: 208-307) expressed in E. Coli.

    Isotype

    IgG2b
  • Indications d'application

    ELISA: 1/10000

    FCM: 1/200 - 1/400

    ICC: 1/200 - 1/1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified antibody in PBS with 0.05 % 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

    4 °C,-20 °C

    Stockage commentaire

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Antigène

    UFD1L (Ubiquitin Fusion Degradation Protein 1 Homolog (UFD1L))

    Autre désignation

    UFD1L

    Sujet

    The protein encoded by this gene forms a complex with two other proteins, nuclear protein localization-4 and valosin-containing protein, and this complex is necessary for the degradation of ubiquitinated proteins. In addition, this complex controls the disassembly of the mitotic spindle and the formation of a closed nuclear envelope after mitosis. Mutations in this gene have been associated with Catch 22 syndrome as well as cardiac and craniofacial defects. Alternative splicing results in multiple transcript variants encoding different isoforms. A related pseudogene has been identified on chromosome 18.

    Poids moléculaire

    34.5 kDa

    ID gène

    7353

    UniProt

    Q92890
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