UFD1L anticorps

N° du produit ABIN7011379

Détail du produit anti-UFD1L anticorps

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: Immunofluorescence (IF)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant fusion protein of human UFD1L (NP_005650.2).

Isotype: IgG

Information d'application

Indications d'application: IF 1:50-1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 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.

Détails sur UFD1L

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

Autre désignation: UFD1L (UFD1L Produits)

Synonymes: anticorps UFD1, anticorps Ufd1, anticorps ufd1, anticorps wu:fc55f04, anticorps zgc:92341, anticorps Ufd1l, anticorps ubiquitin recognition factor in ER associated degradation 1, anticorps ubiquitin recognition factor in ER-associated degradation 1, anticorps ubiquitin fusion degradation 1 like (yeast), anticorps ubiquitin recognition factor in ER associated degradation 1 S homeolog, anticorps ubiquitin fusion degradation protein 1 homolog, anticorps Ubiquitin Fusion Degradation (yeast UFD homolog), anticorps UFD1, anticorps Ufd1, anticorps UFD1L, anticorps ufd1.S, anticorps ufd1l, anticorps ufd1, anticorps EHI_125920, anticorps LOC100166745, anticorps LOC100635687, anticorps LOC100648660, anticorps ufd-1

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.

ID gène: 7353

UniProt: Q92890