UFD1L Antikörper

Produktnummer ABIN6570708

Produktdetails anti-UFD1L Antikörper

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

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser UFD1L Antikörper ist unkonjugiert

Applikation: Immunofluorescence (IF)

Aufreinigung: Affinity purification

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

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF 1:50-1:200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu UFD1L

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

Andere Bezeichnung: UFD1L (UFD1L Produkte)

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

Hintergrund: 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.

Molekulargewicht:

Observed_MW: 38kDa

Calculated_MW: 29kDa/34kDa/38kDa

Gen-ID: 7353

UniProt: Q92890