UFD1L anticorps

N° du produit ABIN5698664

L’anticorps Lapin Polyclonal anti-UFD1L a été validé pour WB, IHC, ELISA, IF et IP. Il convient pour détecter UFD1L dans des échantillons de Humain, Souris et Rat.

Aperçu rapide pour UFD1L anticorps (ABIN5698664)

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp UFD1L est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF), Immunoprecipitation (IP)

Détail du produit anti-UFD1L anticorps

Fonction: UFD1 antibody

Immunogène: ubiquitin fusion degradation 1 like (yeast)

Isotype: IgG

Information d'application

Indications d'application: WB : 1:500-1:5000,IHC:1:20-1:200,IP:1:50O-1:5000,IF:1:10-1:100

Commentaires:

mouse thymus tissue were subjected to SDS PAGE followed by western blot with FNab09233( UFD1L Antibody) at dilution of 1:1000

Restrictions: For Research Use only

Stockage

Buffer: PBS with 0.02 % sodium azide and 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.

Conseil sur la manipulation: Avoid repeated freeze / thaw cycles.

Stock: -20 °C

Stockage commentaire: -20°C for 12 months

Date de péremption: 12 months

Détails sur UFD1L

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

Autre désignation: UFD1

Sujet:

Synonyms: Ubiquitin recognition factor in ER-associated degradation protein 1|Ubiquitin fusion degradation protein 1 (UB fusion protein 1)|UFD1|UFD1L

Background: 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: 20kDa

ID gène: 7353

UniProt: Q92890